ENST00000305242.10:c.2675C>A
MANE Select
|
ENSP00000306410.5:p.Ser892Ter
|
|
ENST00000672841.1:c.1751C>A
|
ENSP00000499983.1:p.Ser584Ter
|
|
ENST00000672877.1:c.1250C>A
|
ENSP00000500120.1:p.Ser417Ter
|
|
ENST00000673384.1:c.1751C>A
|
ENSP00000500856.1:p.Ser584Ter
|
|
ENST00000673439.1:c.2675C>A
|
ENSP00000500782.1:p.Ser892Ter
|
|
ENST00000305242.9:c.2675C>A
|
ENSP00000306410.5:p.Ser892Ter
|
|
NM_001290020.1:c.2675C>A
|
NP_001276949.1:p.Ser892Ter
|
|
NM_001290021.1:c.1250C>A
|
NP_001276950.1:p.Ser417Ter
|
|
NM_001312689.1:c.1751C>A
|
NP_001299618.1:p.Ser584Ter
|
|
NM_018076.3:c.2675C>A
|
NP_060546.2:p.Ser892Ter
|
|
NM_018076.4:c.2675C>A
|
NP_060546.2:p.Ser892Ter
|
|
XM_011519526.1:c.2675C>A
|
XP_011517828.1:p.Ser892Ter
|
|
XM_011519527.1:c.2675C>A
|
XP_011517829.1:p.Ser892Ter
|
|
XM_011519528.1:c.2675C>A
|
XP_011517830.1:p.Ser892Ter
|
|
XM_011519529.1:c.2675C>A
|
XP_011517831.1:p.Ser892Ter
|
|
XM_011519530.1:c.2675C>A
|
XP_011517832.1:p.Ser892Ter
|
|
XM_011519531.1:c.2675C>A
|
XP_011517833.1:p.Ser892Ter
|
|
XM_011519532.1:c.2465C>A
|
XP_011517834.1:p.Ser822Ter
|
|
XM_011519533.1:c.1751C>A
|
XP_011517835.1:p.Ser584Ter
|
|
XM_011519534.1:c.1751C>A
|
XP_011517836.1:p.Ser584Ter
|
|
XM_011519535.1:c.1589C>A
|
XP_011517837.1:p.Ser530Ter
|
|
XM_011519537.1:c.1250C>A
|
XP_011517839.1:p.Ser417Ter
|
|
XM_024448049.1:c.2804C>A
|
XP_024303817.1:p.Ser935Ter
|
|
XM_024448050.1:c.2804C>A
|
XP_024303818.1:p.Ser935Ter
|
|
XM_024448051.1:c.2804C>A
|
XP_024303819.1:p.Ser935Ter
|
|
XM_024448052.1:c.2804C>A
|
XP_024303820.1:p.Ser935Ter
|
|
XM_024448053.1:c.2804C>A
|
XP_024303821.1:p.Ser935Ter
|
|
XM_024448054.1:c.2594C>A
|
XP_024303822.1:p.Ser865Ter
|
|
XM_024448055.1:c.1880C>A
|
XP_024303823.1:p.Ser627Ter
|
|
XM_024448056.1:c.1880C>A
|
XP_024303824.1:p.Ser627Ter
|
|
XM_024448057.1:c.1718C>A
|
XP_024303825.1:p.Ser573Ter
|
|
XM_024448058.1:c.1379C>A
|
XP_024303826.1:p.Ser460Ter
|
|
NM_001290020.2:c.2675C>A
|
NP_001276949.1:p.Ser892Ter
|
|
NM_001290021.2:c.1250C>A
|
NP_001276950.1:p.Ser417Ter
|
|
NM_001312689.2:c.1751C>A
|
NP_001299618.1:p.Ser584Ter
|
|
NM_018076.5:c.2675C>A
MANE Select
|
NP_060546.2:p.Ser892Ter
|
|