ENST00000348974.5:c.907G>T
|
ENSP00000330021.7:p.Ala303Ser
|
|
ENST00000394236.9:c.907G>T
MANE Select
|
ENSP00000377783.3:p.Ala303Ser
|
|
ENST00000407433.6:c.862G>T
|
ENSP00000385794.2:p.Ala288Ser
|
|
ENST00000647936.1:c.907G>T
|
ENSP00000496822.1:p.Ala303Ser
|
|
ENST00000648381.1:n.1075G>T
|
|
|
ENST00000648853.1:c.865G>T
|
ENSP00000497262.1:p.Ala289Ser
|
|
ENST00000649103.1:c.1006G>T
|
ENSP00000497962.1:n.1006G>T
|
|
ENST00000650591.1:c.1003G>T
|
ENSP00000497376.1:p.Ala335Ser
|
|
ENST00000394236.7:c.907G>T
|
ENSP00000377783.3:p.Ala303Ser
|
|
ENST00000407433.5:c.514G>T
|
ENSP00000385794.1:p.Ala172Ser
|
|
NM_000313.3:c.907G>T , LRG_572t1:c.907G>T
|
NP_000304.2:p.Ala303Ser
|
|
NM_001314077.1:c.1003G>T , LRG_572t2:c.1003G>T
|
NP_001301006.1:p.Ala335Ser
|
|
NM_000313.4:c.907G>T
MANE Select
|
NP_000304.2:p.Ala303Ser
|
|
NM_001314077.2:c.1003G>T
|
NP_001301006.1:p.Ala335Ser
|
|