ENST00000262493.12:c.870A=
MANE Select
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ENSP00000262493.6:p.Glu290=
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ENST00000562316.6:c.537A=
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ENSP00000457238.2:p.Glu179=
|
|
ENST00000564727.2:c.174A=
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ENSP00000454971.2:p.Glu58=
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ENST00000568375.2:c.116-3336A=
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|
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ENST00000638185.1:n.1085A=
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|
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ENST00000638210.1:n.1170A=
|
|
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ENST00000638705.1:c.870A=
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ENSP00000491223.1:p.Glu290=
|
|
ENST00000638836.1:n.780A=
|
|
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ENST00000639055.1:n.1591A=
|
|
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ENST00000639251.1:n.771A=
|
|
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ENST00000639268.1:c.505A=
|
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ENST00000639341.1:c.395A=
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ENST00000639770.1:c.908A=
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ENSP00000491999.1:n.908A=
|
|
ENST00000640390.1:n.800A=
|
|
|
ENST00000640469.1:c.234A=
|
ENSP00000491875.1:p.Glu78=
|
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ENST00000640560.1:n.646A=
|
|
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ENST00000640893.1:c.*268A=
|
ENSP00000492677.1:n.*268A=
|
|
ENST00000262493.10:c.870A=
|
ENSP00000262493.6:p.Glu290=
|
|
ENST00000564727.1:c.90A=
|
ENSP00000454971.1:p.Glu30=
|
|
ENST00000568375.1:n.116-3336A=
|
|
|
NM_020988.2:c.870A=
|
NP_066268.1:p.Glu290=
|
|
XM_011523003.1:c.744A=
|
XP_011521305.1:p.Glu248=
|
|
XM_011523003.3:c.744A=
|
XP_011521305.1:p.Glu248=
|
|
NM_020988.3:c.870A=
MANE Select
|
NP_066268.1:p.Glu290=
|
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