ENST00000682012.1:n.786G>C
|
|
|
ENST00000684569.1:n.642G>C
|
|
|
ENST00000561421.6:c.597G>C
MANE Select
|
ENSP00000453347.2:p.Glu199Asp
|
|
ENST00000646551.1:n.2224G>C
|
|
|
ENST00000261755.9:c.597G>C
|
ENSP00000261755.5:p.Glu199Asp
|
|
ENST00000407106.5:c.597G>C
|
ENSP00000385080.1:p.Glu199Asp
|
|
ENST00000539156.5:c.387G>C
|
ENSP00000454271.1:p.Glu129Asp
|
|
ENST00000558514.1:n.143G>C
|
|
|
ENST00000558627.1:n.525G>C
|
|
|
ENST00000561421.5:c.597G>C
|
ENSP00000453347.1:p.Glu199Asp
|
|
NM_000137.2:c.597G>C
|
NP_000128.1:p.Glu199Asp
|
|
XM_024449872.1:c.597G>C
|
XP_024305640.1:p.Glu199Asp
|
|
NM_000137.4:c.597G>C
MANE Select
|
NP_000128.1:p.Glu199Asp
|
|
NM_001374377.1:c.597G>C
|
NP_001361306.1:p.Glu199Asp
|
|
NM_001374380.1:c.597G>C
|
NP_001361309.1:p.Glu199Asp
|
|