ENST00000347132.10:c.277C>T
MANE Select
|
ENSP00000262916.6:p.Arg93Trp
|
|
ENST00000347132.9:c.277C>T
|
ENSP00000262916.6:p.Arg93Trp
|
|
ENST00000509682.6:c.277C>T
|
ENSP00000423756.2:p.Arg93Trp
|
|
NM_004700.3:c.277C>T
|
NP_004691.2:p.Arg93Trp
|
|
NM_172163.2:c.277C>T
|
NP_751895.1:p.Arg93Trp
|
|
XM_011542417.1:c.277C>T
|
XP_011540719.1:p.Arg93Trp
|
|
XM_011542418.1:c.277C>T
|
XP_011540720.1:p.Arg93Trp
|
|
XM_011542419.1:c.277C>T
|
XP_011540721.1:p.Arg93Trp
|
|
XM_011542420.1:c.277C>T
|
XP_011540722.1:p.Arg93Trp
|
|
XR_946798.1:n.283C>T
|
|
|
XR_946799.1:n.283C>T
|
|
|
XR_946800.1:n.283C>T
|
|
|
NM_004700.4:c.277C>T
MANE Select
|
NP_004691.2:p.Arg93Trp
|
|
NM_172163.3:c.277C>T
|
NP_751895.1:p.Arg93Trp
|
|