ENST00000647941.2:c.726C>T
MANE Select
|
ENSP00000497326.1:p.Gly242=
|
|
ENST00000264193.2:c.726C>T
|
ENSP00000264193.2:p.Gly242=
|
|
ENST00000513674.1:c.*34-60C>T
|
ENSP00000424924.1:n.*34-60C>T
|
|
ENST00000515041.1:n.832C>T
|
|
|
NM_000097.5:c.726C>T
|
NP_000088.3:p.Gly242=
|
|
XM_005247125.3:c.726C>T
|
XP_005247182.1:p.Gly242=
|
|
XM_011512437.1:c.726C>T
|
XP_011510739.1:p.Gly242=
|
|
NM_000097.7:c.726C>T
MANE Select
|
NP_000088.3:p.Gly242=
|
|
XM_005247125.4:c.726C>T
|
XP_005247182.1:p.Gly242=
|
|
XR_001740025.2:n.897C>T
|
|
|
XR_001740026.1:n.902C>T
|
|
|
XR_001740027.1:n.906C>T
|
|
|
XR_001740028.1:n.906C>T
|
|
|