ENST00000272895.12:c.3608T>G
MANE Select
|
ENSP00000272895.7:p.Val1203Gly
|
|
ENST00000272895.11:c.3608T>G
|
ENSP00000272895.7:p.Val1203Gly
|
|
ENST00000389661.4:c.2654T>G
|
ENSP00000374312.4:p.Val885Gly
|
|
NM_015657.3:c.2654T>G
|
NP_056472.2:p.Val885Gly
|
|
NM_173076.2:c.3608T>G
|
NP_775099.2:p.Val1203Gly
|
|
NR_103740.1:n.3908T>G
|
|
|
XM_011510951.1:c.3608T>G
|
XP_011509253.1:p.Val1203Gly
|
|
XM_011510952.1:c.3608T>G
|
XP_011509254.1:p.Val1203Gly
|
|
XM_011510951.2:c.3608T>G
|
XP_011509253.1:p.Val1203Gly
|
|
NM_173076.3:c.3608T>G
MANE Select
|
NP_775099.2:p.Val1203Gly
|
|
NR_103740.2:n.4106T>G
|
|
|
NM_015657.4:c.2654T>G
|
NP_056472.2:p.Val885Gly
|
|