ENST00000624552.4:c.14899C>G
|
ENSP00000485357.2:p.Arg4967Gly
|
|
ENST00000683500.2:c.14956C>G
MANE Select
|
ENSP00000508292.2:p.Arg4986Gly
|
|
ENST00000623487.1:n.3302C>G
|
|
|
ENST00000624552.3:c.14896C>G
|
ENSP00000485357.1:p.Arg4966Gly
|
|
NM_001291815.1:c.14956C>G
|
NP_001278744.1:p.Arg4986Gly
|
|
XM_011518465.1:c.14833C>G
|
XP_011516767.1:p.Arg4945Gly
|
|
XM_011518466.1:c.14824C>G
|
XP_011516768.1:p.Arg4942Gly
|
|
XM_011518467.1:c.14779C>G
|
XP_011516769.1:p.Arg4927Gly
|
|
NM_001291815.2:c.14956C>G
MANE Select
|
NP_001278744.1:p.Arg4986Gly
|
|
XM_011518465.2:c.14833C>G
|
XP_011516767.1:p.Arg4945Gly
|
|
XM_011518466.2:c.14824C>G
|
XP_011516768.1:p.Arg4942Gly
|
|
XM_011518467.2:c.14779C>G
|
XP_011516769.1:p.Arg4927Gly
|
|
XM_017014585.1:c.11737C>G
|
XP_016870074.1:p.Arg3913Gly
|
|
XM_017014586.1:c.7534C>G
|
XP_016870075.1:p.Arg2512Gly
|
|
XR_001746957.1:n.92+212G>C
|
|
|
XR_001746958.1:n.92+212G>C
|
|
|