ENST00000558767.6:c.441G>C
|
ENSP00000507680.1:p.Ala147=
|
|
ENST00000682012.1:n.516G>C
|
|
|
ENST00000683593.1:n.2104G>C
|
|
|
ENST00000684363.1:c.365-70G>C
|
ENSP00000507314.1:n.365-70G>C
|
|
ENST00000684569.1:n.486G>C
|
|
|
ENST00000561421.6:c.441G>C
MANE Select
|
ENSP00000453347.2:p.Ala147=
|
|
ENST00000646551.1:n.1928G>C
|
|
|
ENST00000261755.9:c.441G>C
|
ENSP00000261755.5:p.Ala147=
|
|
ENST00000407106.5:c.441G>C
|
ENSP00000385080.1:p.Ala147=
|
|
ENST00000537726.5:n.587G>C
|
|
|
ENST00000539156.5:c.231G>C
|
ENSP00000454271.1:p.Ala77=
|
|
ENST00000558022.5:c.441G>C
|
ENSP00000453152.1:p.Ala147=
|
|
ENST00000558627.1:n.369G>C
|
|
|
ENST00000558767.5:n.702G>C
|
|
|
ENST00000561369.1:n.585G>C
|
|
|
ENST00000561421.5:c.441G>C
|
ENSP00000453347.1:p.Ala147=
|
|
NM_000137.2:c.441G>C
|
NP_000128.1:p.Ala147=
|
|
XM_024449872.1:c.441G>C
|
XP_024305640.1:p.Ala147=
|
|
NM_000137.4:c.441G>C
MANE Select
|
NP_000128.1:p.Ala147=
|
|
NM_001374377.1:c.441G>C
|
NP_001361306.1:p.Ala147=
|
|
NM_001374380.1:c.441G>C
|
NP_001361309.1:p.Ala147=
|
|