ENST00000519602.6:c.561G>C
MANE Select
|
ENSP00000430055.2:p.Glu187Asp
|
|
ENST00000323997.10:c.561G>C
|
ENSP00000324105.6:p.Glu187Asp
|
|
ENST00000518175.1:c.561G>C
|
ENSP00000431087.1:p.Glu187Asp
|
|
ENST00000519584.5:c.432G>C
|
ENSP00000430636.1:p.Glu144Asp
|
|
ENST00000519602.5:c.561G>C
|
ENSP00000430055.1:p.Glu187Asp
|
|
ENST00000520221.5:c.561G>C
|
ENSP00000467444.1:p.Glu187Asp
|
|
ENST00000521659.5:c.*507G>C
|
ENSP00000430554.1:n.*507G>C
|
|
ENST00000522301.5:c.561G>C
|
ENSP00000465697.1:p.Glu187Asp
|
|
NM_001193503.1:c.432G>C
|
NP_001180432.1:p.Glu144Asp
|
|
NM_001976.4:c.561G>C
|
NP_001967.3:p.Glu187Asp
|
|
NM_053013.3:c.561G>C
|
NP_443739.3:p.Glu187Asp
|
|
XM_005256521.2:c.588G>C
|
XP_005256578.1:p.Glu196Asp
|
|
XM_011523729.1:c.561G>C
|
XP_011522031.1:p.Glu187Asp
|
|
XM_017024346.2:c.561G>C
|
XP_016879835.1:p.Glu187Asp
|
|
NM_001193503.2:c.432G>C
|
NP_001180432.1:p.Glu144Asp
|
|
NM_001374523.1:c.561G>C
|
NP_001361452.1:p.Glu187Asp
|
|
NM_001374524.1:c.588G>C
|
NP_001361453.1:p.Glu196Asp
|
|
NM_001976.5:c.561G>C
|
NP_001967.3:p.Glu187Asp
|
|
NM_053013.4:c.561G>C
MANE Select
|
NP_443739.3:p.Glu187Asp
|
|