ENST00000642418.1:n.1519G=
|
|
|
ENST00000643693.1:n.983G=
|
|
|
ENST00000644795.1:c.973G=
|
ENSP00000495720.1:p.Glu325=
|
|
ENST00000646782.1:n.1915G=
|
|
|
ENST00000647165.2:c.9181G=
MANE Select
|
ENSP00000495481.1:p.Glu3061=
|
|
ENST00000651214.1:n.1686G=
|
|
|
ENST00000205890.9:c.9181G=
|
ENSP00000205890.5:p.Glu3061=
|
|
ENST00000418233.7:c.973G=
|
ENSP00000408800.3:p.Glu325=
|
|
ENST00000433411.7:n.118G=
|
|
|
ENST00000445289.6:n.316+1399G=
|
|
|
ENST00000556535.5:c.43G=
|
ENSP00000451782.1:p.Glu15=
|
|
ENST00000557190.5:n.83G=
|
|
|
ENST00000557655.5:c.43G=
|
ENSP00000451925.1:p.Glu15=
|
|
ENST00000578472.5:c.43G=
|
ENSP00000467989.1:p.Glu15=
|
|
ENST00000615845.4:c.9181G=
|
ENSP00000481642.1:p.Glu3061=
|
|
NM_016239.3:c.9181G=
|
NP_057323.3:p.Glu3061=
|
|
XM_011523921.1:c.9175G=
|
XP_011522223.1:p.Glu3059=
|
|
XM_017024714.2:c.9121G=
|
XP_016880203.1:p.Glu3041=
|
|
XM_017024715.2:c.9184G=
|
XP_016880204.1:p.Glu3062=
|
|
NM_016239.4:c.9181G=
MANE Select
|
NP_057323.3:p.Glu3061=
|
|