|
ENST00000216465.10:c.193G>C
MANE Select
|
ENSP00000216465.5:p.Asp65His
|
|
|
ENST00000216465.9:c.193G>C
|
ENSP00000216465.5:p.Asp65His
|
|
|
ENST00000349555.7:c.193G>C
|
ENSP00000314404.5:p.Asp65His
|
|
|
ENST00000361389.8:c.28G>C
|
ENSP00000354959.4:p.Asp10His
|
|
|
ENST00000393734.5:c.28G>C
|
ENSP00000377335.1:p.Asp10His
|
|
|
ENST00000553431.5:n.324G>C
|
|
|
|
ENST00000553586.5:c.196G>C
|
ENSP00000451976.1:p.Asp66His
|
|
|
ENST00000553838.5:n.363G>C
|
|
|
|
ENST00000554279.5:c.174+19G>C
|
ENSP00000452498.1:n.174+19G>C
|
|
|
ENST00000554846.5:c.28G>C
|
ENSP00000452531.1:p.Asp10His
|
|
|
ENST00000555093.1:n.4242G>C
|
|
|
|
ENST00000555583.1:c.28G>C
|
ENSP00000452346.1:p.Asp10His
|
|
|
ENST00000556627.5:c.136-383G>C
|
ENSP00000450487.1:n.136-383G>C
|
|
|
ENST00000556914.5:n.273G>C
|
|
|
|
ENST00000557053.5:c.28G>C
|
ENSP00000451150.1:p.Asp10His
|
|
|
ENST00000557639.5:c.28G>C
|
ENSP00000451927.1:p.Asp10His
|
|
|
NM_001312660.1:c.28G>C
|
NP_001299589.1:p.Asp10His
|
|
|
NM_001513.3:c.28G>C
|
NP_001504.2:p.Asp10His
|
|
|
NM_145870.2:c.193G>C
|
NP_665877.1:p.Asp65His
|
|
|
NM_145871.2:c.193G>C
|
NP_665878.2:p.Asp65His
|
|
|
XM_005267559.2:c.28G>C
|
XP_005267616.1:p.Asp10His
|
|
|
XM_011536670.1:c.-284G>C
|
XP_011534972.1:n.-284G>C
|
|
|
XM_011536671.1:c.196G>C
|
XP_011534973.1:p.Asp66His
|
|
|
NM_001363703.1:c.196G>C
|
NP_001350632.1:p.Asp66His
|
|
|
XM_011536670.2:c.-284G>C
|
XP_011534972.1:n.-284G>C
|
|
|
XM_011536671.2:c.196G>C
|
XP_011534973.1:p.Asp66His
|
|
|
XM_024449549.1:c.-284G>C
|
XP_024305317.1:n.-284G>C
|
|
|
XM_024449550.1:c.28G>C
|
XP_024305318.1:p.Asp10His
|
|
|
XM_024449551.1:c.28G>C
|
XP_024305319.1:p.Asp10His
|
|
|
XM_024449552.1:c.28G>C
|
XP_024305320.1:p.Asp10His
|
|
|
NM_145870.3:c.193G>C
MANE Select
|
NP_665877.1:p.Asp65His
|
|
|
NM_001312660.2:c.28G>C
|
NP_001299589.1:p.Asp10His
|
|
|
NM_001363703.2:c.196G>C
|
NP_001350632.1:p.Asp66His
|
|
|
NM_145871.3:c.193G>C
|
NP_665878.2:p.Asp65His
|
|
