ENST00000261937.11:c.3984A>G
MANE Select
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ENSP00000261937.6:p.Gly1328=
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ENST00000261937.10:c.3984A>G
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ENSP00000261937.6:p.Gly1328=
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ENST00000502603.5:n.684A>G
|
|
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NM_182925.4:c.3984A>G
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NP_891555.2:p.Gly1328=
|
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XM_011534477.1:c.4233A>G
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XP_011532779.1:p.Gly1411=
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|
XM_011534478.1:c.4215A>G
|
XP_011532780.1:p.Gly1405=
|
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XM_011534482.1:c.4002A>G
|
XP_011532784.1:p.Gly1334=
|
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XM_011534483.1:c.3924A>G
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XP_011532785.1:p.Gly1308=
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XM_011534484.1:c.3525A>G
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XP_011532786.1:p.Gly1175=
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XR_941095.1:n.4270A>G
|
|
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XM_011534478.3:c.4215A>G
|
XP_011532780.1:p.Gly1405=
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XM_011534484.2:c.3525A>G
|
XP_011532786.1:p.Gly1175=
|
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XM_017009263.1:c.*130A>G
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XP_016864752.1:n.*130A>G
|
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XM_017009268.1:c.3906A>G
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XP_016864757.1:p.Gly1302=
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XR_001742050.2:n.4474A>G
|
|
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NM_182925.5:c.3984A>G
MANE Select
|
NP_891555.2:p.Gly1328=
|
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