ENST00000261304.7:c.1841G>C
MANE Select
|
ENSP00000261304.2:p.Trp614Ser
|
|
ENST00000261304.6:c.1841G>C
|
ENSP00000261304.2:p.Trp614Ser
|
|
ENST00000393568.8:c.1772G>C
|
ENSP00000377198.4:p.Trp591Ser
|
|
ENST00000393569.6:c.1763G>C
|
ENSP00000377199.2:p.Trp588Ser
|
|
ENST00000544807.6:c.1673G>C
|
ENSP00000437513.2:p.Trp558Ser
|
|
ENST00000555000.5:c.1208G>C
|
ENSP00000450472.1:p.Trp403Ser
|
|
ENST00000555179.1:c.377G>C
|
|
|
NM_000153.3:c.1841G>C
|
NP_000144.2:p.Trp614Ser
|
|
NM_001201401.1:c.1772G>C
|
NP_001188330.1:p.Trp591Ser
|
|
NM_001201402.1:c.1763G>C
|
NP_001188331.1:p.Trp588Ser
|
|
XM_011536618.1:c.1673G>C
|
XP_011534920.1:p.Trp558Ser
|
|
XM_011536618.2:c.1673G>C
|
XP_011534920.1:p.Trp558Ser
|
|
NM_000153.4:c.1841G>C
MANE Select
|
NP_000144.2:p.Trp614Ser
|
|
NM_001201401.2:c.1772G>C
|
NP_001188330.1:p.Trp591Ser
|
|
NM_001201402.2:c.1763G>C
|
NP_001188331.1:p.Trp588Ser
|
|