ENST00000368373.8:c.1316G=
MANE Select
|
ENSP00000357357.3:p.Ser439=
|
|
ENST00000327247.9:c.1316G=
|
ENSP00000314508.5:p.Ser439=
|
|
ENST00000368373.7:c.1316G=
|
ENSP00000357357.3:p.Ser439=
|
|
ENST00000427500.7:c.1169G=
|
ENSP00000402577.2:p.Ser390=
|
|
ENST00000428024.3:c.1055G=
|
ENSP00000397986.2:p.Ser352=
|
|
ENST00000464536.1:n.83G=
|
|
|
ENST00000478472.1:n.307G=
|
|
|
ENST00000484489.5:n.475G=
|
|
|
NM_000157.3:c.1316G=
|
NP_000148.2:p.Ser439=
|
|
NM_001005741.2:c.1316G=
|
NP_001005741.1:p.Ser439=
|
|
NM_001005742.2:c.1316G=
|
NP_001005742.1:p.Ser439=
|
|
NM_001171811.1:c.1055G=
|
NP_001165282.1:p.Ser352=
|
|
NM_001171812.1:c.1169G=
|
NP_001165283.1:p.Ser390=
|
|
XM_006711270.1:c.1316G=
|
XP_006711333.1:p.Ser439=
|
|
XM_011509407.1:c.1316G=
|
XP_011507709.1:p.Ser439=
|
|
NM_000157.4:c.1316G=
MANE Select
|
NP_000148.2:p.Ser439=
|
|
NM_001005741.3:c.1316G=
|
NP_001005741.1:p.Ser439=
|
|
NM_001005742.3:c.1316G=
|
NP_001005742.1:p.Ser439=
|
|
NM_001171811.2:c.1055G=
|
NP_001165282.1:p.Ser352=
|
|
NM_001171812.2:c.1169G=
|
NP_001165283.1:p.Ser390=
|
|