ENST00000624552.4:c.14848C>T
|
ENSP00000485357.2:p.Arg4950Trp
|
|
ENST00000683500.2:c.14905C>T
MANE Select
|
ENSP00000508292.2:p.Arg4969Trp
|
|
ENST00000623487.1:n.3251C>T
|
|
|
ENST00000624552.3:c.14845C>T
|
ENSP00000485357.1:p.Arg4949Trp
|
|
NM_001291815.1:c.14905C>T
|
NP_001278744.1:p.Arg4969Trp
|
|
XM_011518465.1:c.14782C>T
|
XP_011516767.1:p.Arg4928Trp
|
|
XM_011518466.1:c.14773C>T
|
XP_011516768.1:p.Arg4925Trp
|
|
XM_011518467.1:c.14728C>T
|
XP_011516769.1:p.Arg4910Trp
|
|
NM_001291815.2:c.14905C>T
MANE Select
|
NP_001278744.1:p.Arg4969Trp
|
|
XM_011518465.2:c.14782C>T
|
XP_011516767.1:p.Arg4928Trp
|
|
XM_011518466.2:c.14773C>T
|
XP_011516768.1:p.Arg4925Trp
|
|
XM_011518467.2:c.14728C>T
|
XP_011516769.1:p.Arg4910Trp
|
|
XM_017014585.1:c.11686C>T
|
XP_016870074.1:p.Arg3896Trp
|
|
XM_017014586.1:c.7483C>T
|
XP_016870075.1:p.Arg2495Trp
|
|
XR_001746957.1:n.92+263G>A
|
|
|
XR_001746958.1:n.92+263G>A
|
|
|