|
ENST00000646891.2:c.1432+311A=
MANE Select
|
ENSP00000493543.1:n.1432+311A=
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|
|
ENST00000288602.11:c.1552+311A=
|
ENSP00000288602.7:n.1552+311A=
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ENST00000479537.6:c.102+311A=
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ENST00000496384.7:c.1432+311A=
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ENSP00000419060.2:n.1432+311A=
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ENST00000497784.2:c.*882+311A=
|
ENSP00000420119.2:n.*882+311A=
|
|
|
ENST00000642228.1:c.*510+311A=
|
ENSP00000493678.1:n.*510+311A=
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ENST00000642875.1:n.874+311A=
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ENST00000644120.1:n.1822+311A=
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ENST00000644650.1:c.528+311A=
|
|
|
|
ENST00000644905.1:n.1521+311A=
|
|
|
|
ENST00000644969.2:c.1552+311A=
MANE Plus Clinical
|
ENSP00000496776.1:n.1552+311A=
|
|
|
ENST00000646334.1:n.873A=
|
|
|
|
ENST00000646730.1:c.1432+311A=
|
ENSP00000494784.1:n.1432+311A=
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|
ENST00000646891.1:c.1432+311A=
|
ENSP00000493543.1:n.1432+311A=
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|
ENST00000647434.1:c.475+311A=
|
ENSP00000495132.1:n.475+311A=
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|
|
ENST00000288602.10:c.1432+311A=
|
ENSP00000288602.6:n.1432+311A=
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|
ENST00000496384.6:c.255+311A=
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|
ENST00000497784.1:c.1467+311A=
|
ENSP00000420119.1:n.1467+311A=
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|
NM_004333.4:c.1432+311A= , LRG_299t1:c.1432+311A=
|
NP_004324.2:n.1432+311A=
|
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XM_005250045.1:c.1432+311A=
|
XP_005250102.1:n.1432+311A=
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XM_005250046.1:c.1432+311A=
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XP_005250103.1:n.1432+311A=
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XM_011516529.1:c.1432+311A=
|
XP_011514831.1:n.1432+311A=
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|
XM_011516530.1:c.1432+311A=
|
XP_011514832.1:n.1432+311A=
|
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XR_242190.1:n.1440+311A=
|
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|
XR_927520.1:n.1440+311A=
|
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XR_927521.1:n.1440+311A=
|
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|
XR_927522.1:n.1440+311A=
|
|
|
|
XR_927523.1:n.1440+311A=
|
|
|
|
NM_001354609.1:c.1432+311A=
|
NP_001341538.1:n.1432+311A=
|
|
|
NM_004333.5:c.1432+311A=
|
NP_004324.2:n.1432+311A=
|
|
|
NR_148928.1:n.1737+311A=
|
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|
XM_017012558.1:c.1552+311A=
|
XP_016868047.1:n.1552+311A=
|
|
|
XM_017012559.1:c.1552+311A=
|
XP_016868048.1:n.1552+311A=
|
|
|
XR_001744857.1:n.1560+311A=
|
|
|
|
XR_001744858.1:n.1560+311A=
|
|
|
|
NM_001354609.2:c.1432+311A=
|
NP_001341538.1:n.1432+311A=
|
|
|
NM_001374244.1:c.1552+311A=
|
NP_001361173.1:n.1552+311A=
|
|
|
NM_001374258.1:c.1552+311A=
MANE Plus Clinical
|
NP_001361187.1:n.1552+311A=
|
|
|
NM_004333.6:c.1432+311A=
MANE Select
|
NP_004324.2:n.1432+311A=
|
|
|
NM_001378467.1:c.1441+311A=
|
NP_001365396.1:n.1441+311A=
|
|
|
NM_001378468.1:c.1432+311A=
|
NP_001365397.1:n.1432+311A=
|
|
|
NM_001378469.1:c.1366+311A=
|
NP_001365398.1:n.1366+311A=
|
|
|
NM_001378470.1:c.1330+311A=
|
NP_001365399.1:n.1330+311A=
|
|
|
NM_001378471.1:c.1321+311A=
|
NP_001365400.1:n.1321+311A=
|
|
|
NM_001378472.1:c.1276+311A=
|
NP_001365401.1:n.1276+311A=
|
|
|
NM_001378473.1:c.1276+311A=
|
NP_001365402.1:n.1276+311A=
|
|
|
NM_001378474.1:c.1432+311A=
|
NP_001365403.1:n.1432+311A=
|
|
|
NM_001378475.1:c.1168+311A=
|
NP_001365404.1:n.1168+311A=
|
|
