ENST00000651671.1:c.6506G>A
MANE Select
|
ENSP00000498587.1:p.Gly2169Glu
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ENST00000679595.1:c.*1546G>A
|
ENSP00000506241.1:n.*1546G>A
|
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ENST00000679969.1:n.3102G>A
|
|
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ENST00000680003.1:n.2838G>A
|
|
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ENST00000680133.1:c.6392G>A
|
ENSP00000505319.1:p.Gly2131Glu
|
|
ENST00000680218.1:c.6386G>A
|
ENSP00000505339.1:p.Gly2129Glu
|
|
ENST00000680668.1:c.6392G>A
|
ENSP00000506336.1:p.Gly2131Glu
|
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ENST00000680778.1:c.4103G>A
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ENSP00000506033.1:p.Gly1368Glu
|
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ENST00000680924.1:c.*3906G>A
|
ENSP00000506031.1:n.*3906G>A
|
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ENST00000681135.1:c.*4115G>A
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ENSP00000506636.1:n.*4115G>A
|
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ENST00000681298.1:n.4611G>A
|
|
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ENST00000681454.1:c.*5742G>A
|
ENSP00000505763.1:n.*5742G>A
|
|
ENST00000277541.6:c.6506G>A
|
ENSP00000277541.6:p.Gly2169Glu
|
|
NM_017617.3:c.6506G>A
|
NP_060087.3:p.Gly2169Glu
|
|
XM_011518717.1:c.5807G>A
|
XP_011517019.1:p.Gly1936Glu
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|
NM_017617.5:c.6506G>A
MANE Select
|
NP_060087.3:p.Gly2169Glu
|
|
XM_011518717.2:c.5783G>A
|
XP_011517019.2:p.Gly1928Glu
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