ENST00000642418.1:n.1508A>T
|
|
|
ENST00000643693.1:n.972A>T
|
|
|
ENST00000644795.1:c.962A>T
|
ENSP00000495720.1:p.Glu321Val
|
|
ENST00000646782.1:n.1904A>T
|
|
|
ENST00000647165.2:c.9170A>T
MANE Select
|
ENSP00000495481.1:p.Glu3057Val
|
|
ENST00000651214.1:n.1675A>T
|
|
|
ENST00000205890.9:c.9170A>T
|
ENSP00000205890.5:p.Glu3057Val
|
|
ENST00000418233.7:c.962A>T
|
ENSP00000408800.3:p.Glu321Val
|
|
ENST00000433411.7:n.107A>T
|
|
|
ENST00000445289.6:n.316+1388A>T
|
|
|
ENST00000556535.5:c.32A>T
|
ENSP00000451782.1:p.Glu11Val
|
|
ENST00000557190.5:n.72A>T
|
|
|
ENST00000557655.5:c.32A>T
|
ENSP00000451925.1:p.Glu11Val
|
|
ENST00000578472.5:c.32A>T
|
ENSP00000467989.1:p.Glu11Val
|
|
ENST00000615845.4:c.9170A>T
|
ENSP00000481642.1:p.Glu3057Val
|
|
NM_016239.3:c.9170A>T
|
NP_057323.3:p.Glu3057Val
|
|
XM_011523921.1:c.9164A>T
|
XP_011522223.1:p.Glu3055Val
|
|
XM_017024714.2:c.9110A>T
|
XP_016880203.1:p.Glu3037Val
|
|
XM_017024715.2:c.9173A>T
|
XP_016880204.1:p.Glu3058Val
|
|
NM_016239.4:c.9170A>T
MANE Select
|
NP_057323.3:p.Glu3057Val
|
|