ENST00000368373.8:c.272G=
MANE Select
|
ENSP00000357357.3:p.Ser91=
|
|
ENST00000327247.9:c.272G=
|
ENSP00000314508.5:p.Ser91=
|
|
ENST00000368373.7:c.272G=
|
ENSP00000357357.3:p.Ser91=
|
|
ENST00000427500.7:c.272G=
|
ENSP00000402577.2:p.Ser91=
|
|
ENST00000428024.3:c.11G=
|
ENSP00000397986.2:p.Ser4=
|
|
ENST00000467918.5:n.462G=
|
|
|
ENST00000473570.5:n.593G=
|
|
|
ENST00000484489.5:n.339+52G=
|
|
|
ENST00000493842.5:n.610G=
|
|
|
ENST00000497670.5:n.42G=
|
|
|
NM_000157.3:c.272G=
|
NP_000148.2:p.Ser91=
|
|
NM_001005741.2:c.272G=
|
NP_001005741.1:p.Ser91=
|
|
NM_001005742.2:c.272G=
|
NP_001005742.1:p.Ser91=
|
|
NM_001171811.1:c.11G=
|
NP_001165282.1:p.Ser4=
|
|
NM_001171812.1:c.272G=
|
NP_001165283.1:p.Ser91=
|
|
XM_006711270.1:c.272G=
|
XP_006711333.1:p.Ser91=
|
|
XM_011509407.1:c.272G=
|
XP_011507709.1:p.Ser91=
|
|
NM_000157.4:c.272G=
MANE Select
|
NP_000148.2:p.Ser91=
|
|
NM_001005741.3:c.272G=
|
NP_001005741.1:p.Ser91=
|
|
NM_001005742.3:c.272G=
|
NP_001005742.1:p.Ser91=
|
|
NM_001171811.2:c.11G=
|
NP_001165282.1:p.Ser4=
|
|
NM_001171812.2:c.272G=
|
NP_001165283.1:p.Ser91=
|
|