ENST00000317961.9:c.4057G>T
MANE Select
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ENSP00000322408.4:p.Gly1353Ter
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ENST00000317961.8:c.4057G>T
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ENSP00000322408.4:p.Gly1353Ter
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ENST00000382806.6:c.3886G>T
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ENSP00000372256.2:p.Gly1296Ter
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ENST00000440077.5:c.3934G>T
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ENSP00000398543.1:p.Gly1312Ter
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ENST00000469599.6:n.2655G>T
|
|
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ENST00000492117.1:n.3949G>T
|
|
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ENST00000541639.5:c.4150G>T
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ENSP00000444293.1:p.Gly1384Ter
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NM_001146705.1:c.4150G>T
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NP_001140177.1:p.Gly1384Ter
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NM_001146706.1:c.3886G>T
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NP_001140178.1:p.Gly1296Ter
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NM_004653.4:c.4057G>T
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NP_004644.2:p.Gly1353Ter
|
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XM_005262560.1:c.3922G>T
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XP_005262617.1:p.Gly1308Ter
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XM_005262561.1:c.3826G>T
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XP_005262618.1:p.Gly1276Ter
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XM_011531468.1:c.3979G>T
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XP_011529770.1:p.Gly1327Ter
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XR_244571.2:n.4345G>T
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|
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XR_430568.2:n.4679G>T
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|
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XM_005262560.3:c.3922G>T
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XP_005262617.1:p.Gly1308Ter
|
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XM_005262561.3:c.3826G>T
|
XP_005262618.1:p.Gly1276Ter
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XM_011531468.3:c.3979G>T
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XP_011529770.1:p.Gly1327Ter
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XM_024452495.1:c.2047G>T
|
XP_024308263.1:p.Gly683Ter
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XM_024452496.1:c.1813G>T
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XP_024308264.1:p.Gly605Ter
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XR_001756009.2:n.4795G>T
|
|
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XR_001756010.2:n.4795G>T
|
|
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XR_001756011.2:n.4660G>T
|
|
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XR_001756012.2:n.4808G>T
|
|
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XR_001756013.2:n.4126G>T
|
|
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XR_002958832.1:n.4227G>T
|
|
|
XR_002958834.1:n.4451G>T
|
|
|
XR_002958835.1:n.4334G>T
|
|
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XR_002958836.1:n.5017G>T
|
|
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XR_002958837.1:n.4824G>T
|
|
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XR_244571.4:n.4344G>T
|
|
|
XR_430568.4:n.4678G>T
|
|
|
NM_001146706.2:c.3886G>T
|
NP_001140178.1:p.Gly1296Ter
|
|
NM_004653.5:c.4057G>T
MANE Select
|
NP_004644.2:p.Gly1353Ter
|
|
NM_001146705.2:c.4150G>T
|
NP_001140177.1:p.Gly1384Ter
|
|