ENST00000475778.2:n.1309G=
|
|
|
ENST00000684143.1:c.880G=
|
ENSP00000508264.1:p.Ala294=
|
|
ENST00000684745.1:n.557G=
|
|
|
ENST00000379374.5:c.883G=
MANE Select
|
ENSP00000368682.4:p.Ala295=
|
|
ENST00000379374.4:c.883G=
|
ENSP00000368682.4:p.Ala295=
|
|
ENST00000475778.1:n.156G=
|
|
|
NM_000444.5:c.883G=
|
NP_000435.3:p.Ala295=
|
|
NM_001282754.1:c.883G=
|
NP_001269683.1:p.Ala295=
|
|
XM_011545533.1:c.127G=
|
XP_011543835.1:p.Ala43=
|
|
XM_011545534.1:c.127G=
|
XP_011543836.1:p.Ala43=
|
|
XM_011545535.1:c.883G=
|
XP_011543837.1:p.Ala295=
|
|
XM_017029579.1:c.127G=
|
XP_016885068.1:p.Ala43=
|
|
XM_024452390.1:c.592G=
|
XP_024308158.1:p.Ala198=
|
|
XR_001755695.1:n.1562G=
|
|
|
NM_000444.6:c.883G=
MANE Select
|
NP_000435.3:p.Ala295=
|
|
NM_001282754.2:c.883G=
|
NP_001269683.1:p.Ala295=
|
|