ENST00000373588.9:c.946C>T
MANE Select
|
ENSP00000362690.4:p.Gln316Ter
|
|
ENST00000373587.3:c.298C>T
|
ENSP00000362689.3:p.Gln100Ter
|
|
ENST00000373588.8:c.946C>T
|
ENSP00000362690.4:p.Gln316Ter
|
|
ENST00000620110.4:c.871-1846C>T
|
ENSP00000483309.1:n.871-1846C>T
|
|
NM_004959.4:c.946C>T
|
NP_004950.2:p.Gln316Ter
|
|
XM_005251871.2:c.946C>T
|
XP_005251928.1:p.Gln316Ter
|
|
XM_005251872.3:c.685C>T
|
XP_005251929.1:p.Gln229Ter
|
|
XM_011518455.1:c.946C>T
|
XP_011516757.1:p.Gln316Ter
|
|
XM_011518456.1:c.870+7016C>T
|
XP_011516758.1:n.870+7016C>T
|
|
NM_004959.5:c.946C>T
MANE Select
|
NP_004950.2:p.Gln316Ter
|
|