ENST00000393943.10:c.373G>C
MANE Select
|
ENSP00000377517.4:p.Asp125His
|
|
ENST00000635880.1:c.373G>C
|
ENSP00000489738.1:p.Asp125His
|
|
ENST00000635916.2:n.1148G>C
|
|
|
ENST00000636340.1:c.*222G>C
|
ENSP00000490002.1:n.*222G>C
|
|
ENST00000636408.1:n.177G>C
|
|
|
ENST00000636573.1:c.373G>C
|
ENSP00000490320.1:p.Asp125His
|
|
ENST00000637044.1:c.*147G>C
|
ENSP00000490684.1:n.*147G>C
|
|
ENST00000637827.1:c.373G>C
|
ENSP00000490804.1:p.Asp125His
|
|
ENST00000638112.1:c.373G>C
|
ENSP00000489839.1:p.Asp125His
|
|
ENST00000638159.1:c.418G>C
|
ENSP00000490360.1:p.Asp140His
|
|
ENST00000023897.10:c.373G>C
|
ENSP00000023897.6:p.Asp125His
|
|
ENST00000393943.9:c.373G>C
|
ENSP00000377517.4:p.Asp125His
|
|
ENST00000428797.7:c.373G>C
|
ENSP00000393097.2:p.Asp125His
|
|
ENST00000437025.6:c.373G>C
|
ENSP00000415441.2:p.Asp125His
|
|
ENST00000519542.1:n.137G>C
|
|
|
ENST00000519621.2:c.373G>C
|
ENSP00000430435.2:p.Asp125His
|
|
ENST00000634335.1:c.373G>C
|
ENSP00000489434.1:p.Asp125His
|
|
NM_000806.5:c.373G>C
|
NP_000797.2:p.Asp125His
|
|
NM_001127643.1:c.373G>C
|
NP_001121115.1:p.Asp125His
|
|
NM_001127644.1:c.373G>C
|
NP_001121116.1:p.Asp125His
|
|
NM_001127645.1:c.373G>C
|
NP_001121117.1:p.Asp125His
|
|
NM_001127648.1:c.373G>C
|
NP_001121120.1:p.Asp125His
|
|
NM_001127644.2:c.373G>C
MANE Select
|
NP_001121116.1:p.Asp125His
|
|
NM_001127643.2:c.373G>C
|
NP_001121115.1:p.Asp125His
|
|
NM_001127645.2:c.373G>C
|
NP_001121117.1:p.Asp125His
|
|
NM_001127648.2:c.373G>C
|
NP_001121120.1:p.Asp125His
|
|