ENST00000261195.3:c.997G>T
MANE Select
|
ENSP00000261195.2:p.Glu333Ter
|
|
ENST00000647960.1:c.*999G>T
|
ENSP00000497202.1:n.*999G>T
|
|
ENST00000648372.1:n.924G>T
|
|
|
ENST00000261195.2:c.997G>T
|
ENSP00000261195.2:p.Glu333Ter
|
|
NM_021957.3:c.997G>T
|
NP_068776.2:p.Glu333Ter
|
|
XM_005253352.1:c.997G>T
|
XP_005253409.1:p.Glu333Ter
|
|
XM_005253354.2:c.778G>T
|
XP_005253411.1:p.Glu260Ter
|
|
XM_006719062.2:c.997G>T
|
XP_006719125.1:p.Glu333Ter
|
|
XM_006719063.2:c.766G>T
|
XP_006719126.1:p.Glu256Ter
|
|
NM_021957.4:c.997G>T
MANE Select
|
NP_068776.2:p.Glu333Ter
|
|
XM_006719063.3:c.766G>T
|
XP_006719126.1:p.Glu256Ter
|
|
XM_017019245.2:c.997G>T
|
XP_016874734.1:p.Glu333Ter
|
|
XM_024448960.1:c.997G>T
|
XP_024304728.1:p.Glu333Ter
|
|