ENST00000624552.4:c.14947C>T
|
ENSP00000485357.2:p.Arg4983Cys
|
|
ENST00000683500.2:c.15004C>T
MANE Select
|
ENSP00000508292.2:p.Arg5002Cys
|
|
ENST00000623487.1:n.3350C>T
|
|
|
ENST00000624552.3:c.14944C>T
|
ENSP00000485357.1:p.Arg4982Cys
|
|
NM_001291815.1:c.15004C>T
|
NP_001278744.1:p.Arg5002Cys
|
|
XM_011518465.1:c.14881C>T
|
XP_011516767.1:p.Arg4961Cys
|
|
XM_011518466.1:c.14872C>T
|
XP_011516768.1:p.Arg4958Cys
|
|
XM_011518467.1:c.14827C>T
|
XP_011516769.1:p.Arg4943Cys
|
|
NM_001291815.2:c.15004C>T
MANE Select
|
NP_001278744.1:p.Arg5002Cys
|
|
XM_011518465.2:c.14881C>T
|
XP_011516767.1:p.Arg4961Cys
|
|
XM_011518466.2:c.14872C>T
|
XP_011516768.1:p.Arg4958Cys
|
|
XM_011518467.2:c.14827C>T
|
XP_011516769.1:p.Arg4943Cys
|
|
XM_017014585.1:c.11785C>T
|
XP_016870074.1:p.Arg3929Cys
|
|
XM_017014586.1:c.7582C>T
|
XP_016870075.1:p.Arg2528Cys
|
|
XR_001746957.1:n.92+164G>A
|
|
|
XR_001746958.1:n.92+164G>A
|
|
|