ENST00000624552.4:c.14926C>T
|
ENSP00000485357.2:p.Arg4976Cys
|
|
ENST00000683500.2:c.14983C>T
MANE Select
|
ENSP00000508292.2:p.Arg4995Cys
|
|
ENST00000623487.1:n.3329C>T
|
|
|
ENST00000624552.3:c.14923C>T
|
ENSP00000485357.1:p.Arg4975Cys
|
|
NM_001291815.1:c.14983C>T
|
NP_001278744.1:p.Arg4995Cys
|
|
XM_011518465.1:c.14860C>T
|
XP_011516767.1:p.Arg4954Cys
|
|
XM_011518466.1:c.14851C>T
|
XP_011516768.1:p.Arg4951Cys
|
|
XM_011518467.1:c.14806C>T
|
XP_011516769.1:p.Arg4936Cys
|
|
NM_001291815.2:c.14983C>T
MANE Select
|
NP_001278744.1:p.Arg4995Cys
|
|
XM_011518465.2:c.14860C>T
|
XP_011516767.1:p.Arg4954Cys
|
|
XM_011518466.2:c.14851C>T
|
XP_011516768.1:p.Arg4951Cys
|
|
XM_011518467.2:c.14806C>T
|
XP_011516769.1:p.Arg4936Cys
|
|
XM_017014585.1:c.11764C>T
|
XP_016870074.1:p.Arg3922Cys
|
|
XM_017014586.1:c.7561C>T
|
XP_016870075.1:p.Arg2521Cys
|
|
XR_001746957.1:n.92+185G>A
|
|
|
XR_001746958.1:n.92+185G>A
|
|
|