ENST00000298223.11:c.-13G>C
MANE Select
|
ENSP00000298223.6:n.-13G>C
|
|
ENST00000298223.10:c.-13G>C
|
ENSP00000298223.6:n.-13G>C
|
|
ENST00000321324.11:c.28-1G>C
|
ENSP00000321957.7:n.28-1G>C
|
|
ENST00000449475.6:c.39G>C
|
ENSP00000405638.2:p.Gln13His
|
|
ENST00000454954.6:c.27+1647G>C
|
ENSP00000414094.2:n.27+1647G>C
|
|
ENST00000535625.5:c.-13G>C
|
ENSP00000444794.1:n.-13G>C
|
|
ENST00000536778.5:c.33G>C
|
ENSP00000438568.1:p.Gln11His
|
|
ENST00000538353.1:c.-13G>C
|
ENSP00000440337.1:n.-13G>C
|
|
ENST00000539412.5:c.22-1G>C
|
ENSP00000441547.1:n.22-1G>C
|
|
ENST00000541003.5:c.126G>C
|
ENSP00000443307.1:p.Gln42His
|
|
ENST00000619261.4:c.39G>C
|
ENSP00000480592.1:p.Gln13His
|
|
NM_000803.4:c.-13G>C
|
NP_000794.3:n.-13G>C
|
|
NM_001113534.1:c.-13G>C
|
NP_001107006.1:n.-13G>C
|
|
NM_001113535.1:c.-12-1G>C
|
NP_001107007.1:n.-12-1G>C
|
|
NM_001113536.1:c.-12-1G>C
|
NP_001107008.1:n.-12-1G>C
|
|
XM_005273856.2:c.15G>C
|
XP_005273913.1:p.Gln5His
|
|
XM_011544869.1:c.39G>C
|
XP_011543171.1:p.Gln13His
|
|
XM_011544870.1:c.33G>C
|
XP_011543172.1:p.Gln11His
|
|
XM_011544871.1:c.28-1G>C
|
XP_011543173.1:n.28-1G>C
|
|
XM_011544872.1:c.22-1G>C
|
XP_011543174.1:n.22-1G>C
|
|
XM_005273856.4:c.15G>C
|
XP_005273913.1:p.Gln5His
|
|
XM_024448412.1:c.39G>C
|
XP_024304180.1:p.Gln13His
|
|
NM_000803.5:c.-13G>C
MANE Select
|
NP_000794.3:n.-13G>C
|
|
NM_001113534.2:c.-13G>C
|
NP_001107006.1:n.-13G>C
|
|
NM_001113535.2:c.-12-1G>C
|
NP_001107007.1:n.-12-1G>C
|
|
NM_001113536.2:c.-12-1G>C
|
NP_001107008.1:n.-12-1G>C
|
|