ENST00000388996.10:c.914A>T
MANE Select
|
ENSP00000373648.3:p.Asp305Val
|
|
ENST00000521134.6:c.554A>T
|
ENSP00000429799.1:p.Asp185Val
|
|
ENST00000638588.1:c.587A>T
|
ENSP00000491940.1:p.Asp196Val
|
|
ENST00000639358.1:c.564A>T
|
|
|
ENST00000639496.1:c.587A>T
|
ENSP00000491165.1:p.Asp196Val
|
|
ENST00000388996.8:c.914A>T
|
ENSP00000373648.3:p.Asp305Val
|
|
ENST00000519445.5:c.914A>T
|
ENSP00000428790.1:p.Asp305Val
|
|
ENST00000519589.1:n.692A>T
|
|
|
ENST00000521134.5:c.554A>T
|
ENSP00000429799.1:p.Asp185Val
|
|
ENST00000621976.1:c.551A>T
|
ENSP00000482510.1:p.Asp184Val
|
|
NM_001204824.1:c.554A>T
|
NP_001191753.1:p.Asp185Val
|
|
NM_004519.3:c.914A>T
|
NP_004510.1:p.Asp305Val
|
|
XM_005250914.2:c.-243A>T
|
XP_005250971.1:n.-243A>T
|
|
XM_006716555.2:c.206A>T
|
XP_006716618.1:p.Asp69Val
|
|
XM_011517026.1:c.554A>T
|
XP_011515328.1:p.Asp185Val
|
|
XM_005250914.3:c.-243A>T
|
XP_005250971.1:n.-243A>T
|
|
XM_006716555.3:c.206A>T
|
XP_006716618.1:p.Asp69Val
|
|
XM_011517026.2:c.554A>T
|
XP_011515328.1:p.Asp185Val
|
|
XM_017013400.1:c.692A>T
|
XP_016868889.1:p.Asp231Val
|
|
NM_004519.4:c.914A>T
MANE Select
|
NP_004510.1:p.Asp305Val
|
|
NM_001204824.2:c.554A>T
|
NP_001191753.1:p.Asp185Val
|
|