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NM_024408.4:c.3508G>T
MANE Select
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NP_077719.2:p.Gly1170Ter
|
|
ENST00000256646.7:c.3508G>T
MANE Select
|
ENSP00000256646.2:p.Gly1170Ter
|
|
NM_001200001.1:c.3508G>T
|
NP_001186930.1:p.Gly1170Ter
|
|
NM_001200001.2:c.3508G>T
|
NP_001186930.1:p.Gly1170Ter
|
|
NM_024408.3:c.3508G>T
|
NP_077719.2:p.Gly1170Ter
|
|
ENST00000256646.6:c.3508G>T
|
ENSP00000256646.2:p.Gly1170Ter
|
|
ENST00000478864.1:n.168G>T
|
|
|
XM_005270901.2:c.3391G>T
|
XP_005270958.1:p.Gly1131Ter
|
|
XM_011541519.1:c.3496G>T
|
XP_011539821.1:p.Gly1166Ter
|
|
XM_011541520.1:c.3391G>T
|
XP_011539822.1:p.Gly1131Ter
|