ENST00000398752.11:c.858G>C
MANE Select
|
ENSP00000381736.5:p.Gln286His
|
|
ENST00000282050.6:c.858G>C
|
ENSP00000282050.2:p.Gln286His
|
|
ENST00000398752.10:c.858G>C
|
ENSP00000381736.5:p.Gln286His
|
|
ENST00000586523.1:n.1263G>C
|
|
|
ENST00000586592.5:c.*921G>C
|
ENSP00000466275.3:n.*921G>C
|
|
ENST00000589252.5:c.591G>C
|
ENSP00000466975.1:p.Gln197His
|
|
ENST00000590156.5:c.*754G>C
|
ENSP00000466309.1:n.*754G>C
|
|
ENST00000590665.5:c.792G>C
|
ENSP00000467037.1:p.Gln264His
|
|
ENST00000592364.5:c.227-370G>C
|
ENSP00000468618.1:n.227-370G>C
|
|
ENST00000593152.6:c.708G>C
|
ENSP00000465477.2:p.Gln236His
|
|
NM_001001935.2:c.708G>C
|
NP_001001935.1:p.Gln236His
|
|
NM_001001937.1:c.858G>C
|
NP_001001937.1:p.Gln286His
|
|
NM_001257334.1:c.792G>C
|
NP_001244263.1:p.Gln264His
|
|
NM_001257335.1:c.708G>C
|
NP_001244264.1:p.Gln236His
|
|
NM_004046.5:c.858G>C
|
NP_004037.1:p.Gln286His
|
|
XM_011526018.1:c.708G>C
|
XP_011524320.1:p.Gln236His
|
|
XM_017025789.1:c.858G>C
|
XP_016881278.1:p.Gln286His
|
|
NM_004046.6:c.858G>C
MANE Select
|
NP_004037.1:p.Gln286His
|
|
NM_001001935.3:c.708G>C
|
NP_001001935.1:p.Gln236His
|
|
NM_001257334.2:c.792G>C
|
NP_001244263.1:p.Gln264His
|
|
NM_001001937.2:c.858G>C
|
NP_001001937.1:p.Gln286His
|
|
NM_001257335.2:c.708G>C
|
NP_001244264.1:p.Gln236His
|
|