ENST00000394817.7:c.1197G>C
MANE Select
|
ENSP00000378294.2:p.Gln399His
|
|
ENST00000265195.9:c.1197G>C
|
ENSP00000265195.5:p.Gln399His
|
|
ENST00000394817.6:c.1197G>C
|
ENSP00000378294.2:p.Gln399His
|
|
ENST00000509534.5:c.1218G>C
|
ENSP00000426858.1:p.Gln406His
|
|
ENST00000515008.1:n.532G>C
|
|
|
NM_001037633.1:c.1197G>C
|
NP_001032722.1:p.Gln399His
|
|
NM_022464.4:c.1197G>C
|
NP_071909.1:p.Gln399His
|
|
XM_011543570.1:c.1227G>C
|
XP_011541872.1:p.Gln409His
|
|
XM_011543570.2:c.1227G>C
|
XP_011541872.1:p.Gln409His
|
|
XM_024446164.1:c.1197G>C
|
XP_024301932.1:p.Gln399His
|
|
NM_022464.5:c.1197G>C
MANE Select
|
NP_071909.1:p.Gln399His
|
|
NM_001037633.2:c.1197G>C
|
NP_001032722.1:p.Gln399His
|
|