ENST00000703783.1:n.970A>G
|
|
|
ENST00000703785.1:n.1051A>G
|
|
|
ENST00000262464.9:c.4186A>G
MANE Select
|
ENSP00000262464.4:p.Arg1396Gly
|
|
ENST00000262464.8:c.4186A>G
|
ENSP00000262464.4:p.Arg1396Gly
|
|
ENST00000507835.5:c.736A>G
|
ENSP00000426839.1:p.Arg246Gly
|
|
ENST00000508053.5:c.4186A>G
|
ENSP00000424571.1:p.Arg1396Gly
|
|
ENST00000508989.5:c.4087A>G
|
ENSP00000425596.1:p.Arg1363Gly
|
|
ENST00000619499.4:c.4183A>G
|
ENSP00000482132.1:p.Arg1395Gly
|
|
NM_001999.3:c.4186A>G
|
NP_001990.2:p.Arg1396Gly
|
|
XM_017009228.2:c.4033A>G
|
XP_016864717.1:p.Arg1345Gly
|
|
NM_001999.4:c.4186A>G
MANE Select
|
NP_001990.2:p.Arg1396Gly
|
|