ENST00000261195.3:c.972G>A
MANE Select
|
ENSP00000261195.2:p.Leu324=
|
|
ENST00000647960.1:c.*974G>A
|
ENSP00000497202.1:n.*974G>A
|
|
ENST00000648372.1:n.899G>A
|
|
|
ENST00000261195.2:c.972G>A
|
ENSP00000261195.2:p.Leu324=
|
|
NM_021957.3:c.972G>A
|
NP_068776.2:p.Leu324=
|
|
XM_005253352.1:c.972G>A
|
XP_005253409.1:p.Leu324=
|
|
XM_005253354.2:c.753G>A
|
XP_005253411.1:p.Leu251=
|
|
XM_006719062.2:c.972G>A
|
XP_006719125.1:p.Leu324=
|
|
XM_006719063.2:c.741G>A
|
XP_006719126.1:p.Leu247=
|
|
NM_021957.4:c.972G>A
MANE Select
|
NP_068776.2:p.Leu324=
|
|
XM_006719063.3:c.741G>A
|
XP_006719126.1:p.Leu247=
|
|
XM_017019245.2:c.972G>A
|
XP_016874734.1:p.Leu324=
|
|
XM_024448960.1:c.972G>A
|
XP_024304728.1:p.Leu324=
|
|