ENST00000254108.12:c.527A>G
MANE Select
|
ENSP00000254108.8:p.Asn176Ser
|
|
ENST00000254108.11:c.527A>G
|
ENSP00000254108.7:p.Asn176Ser
|
|
ENST00000380244.7:c.524A>G
|
ENSP00000369594.3:p.Asn175Ser
|
|
ENST00000487509.6:n.592A>G
|
|
|
ENST00000566605.5:c.527A>G
|
ENSP00000455073.1:p.Asn176Ser
|
|
ENST00000568685.1:c.527A>G
|
ENSP00000455282.1:p.Asn176Ser
|
|
NM_001170634.1:c.524A>G
|
NP_001164105.1:p.Asn175Ser
|
|
NM_001170937.1:c.515A>G
|
NP_001164408.1:p.Asn172Ser
|
|
NM_004960.3:c.527A>G , LRG_655t1:c.527A>G
|
NP_004951.1:p.Asn176Ser
|
|
NR_028388.2:n.632A>G
|
|
|
XM_005255233.3:c.-54A>G
|
XP_005255290.1:n.-54A>G
|
|
XM_011545781.1:c.521A>G
|
XP_011544083.1:p.Asn174Ser
|
|
XM_011545782.1:c.-54A>G
|
XP_011544084.1:n.-54A>G
|
|
XM_005255233.5:c.-54A>G
|
XP_005255290.1:n.-54A>G
|
|
XM_011545782.2:c.-54A>G
|
XP_011544084.1:n.-54A>G
|
|
XM_024450221.1:c.518A>G
|
XP_024305989.1:p.Asn173Ser
|
|
NM_004960.4:c.527A>G
MANE Select
|
NP_004951.1:p.Asn176Ser
|
|