ENST00000220420.10:c.1036C>T
MANE Select
|
ENSP00000220420.5:p.Arg346Trp
|
|
ENST00000635871.1:n.505C>T
|
|
|
ENST00000220420.9:c.1036C>T
|
ENSP00000220420.5:p.Arg346Trp
|
|
ENST00000349114.8:c.790C>T
|
ENSP00000220419.8:p.Arg264Trp
|
|
ENST00000396996.3:n.512C>T
|
|
|
ENST00000563838.1:n.269C>T
|
|
|
ENST00000610827.4:c.1033C>T
|
ENSP00000479732.1:p.Arg345Trp
|
|
ENST00000611276.4:c.787C>T
|
ENSP00000482542.1:p.Arg263Trp
|
|
ENST00000622115.1:c.1039C>T
|
ENSP00000479638.1:p.Arg347Trp
|
|
NM_004245.3:c.790C>T
|
NP_004236.1:p.Arg264Trp
|
|
NM_201631.3:c.1036C>T
|
NP_963925.2:p.Arg346Trp
|
|
XM_011522229.1:c.1036C>T
|
XP_011520531.1:p.Arg346Trp
|
|
XM_011522230.1:c.7C>T
|
XP_011520532.1:p.Arg3Trp
|
|
XR_931948.1:n.1210C>T
|
|
|
XM_011522230.2:c.7C>T
|
XP_011520532.1:p.Arg3Trp
|
|
XM_017022729.1:c.7C>T
|
XP_016878218.1:p.Arg3Trp
|
|
NM_004245.4:c.790C>T
|
NP_004236.1:p.Arg264Trp
|
|
NM_201631.4:c.1036C>T
MANE Select
|
NP_963925.2:p.Arg346Trp
|
|