ENST00000576892.8:c.625G>T
MANE Select
|
ENSP00000461135.1:p.Ala209Ser
|
|
ENST00000429336.5:c.193+2009G>T
|
|
|
ENST00000440428.5:c.625G>T
|
ENSP00000402949.2:p.Ala209Ser
|
|
ENST00000576892.7:c.625G>T
|
ENSP00000461135.1:p.Ala209Ser
|
|
ENST00000614850.1:c.277+3466G>T
|
|
|
ENST00000614851.4:c.446G>T
|
|
|
ENST00000620088.4:c.*501G>T
|
ENSP00000484108.1:n.*501G>T
|
|
ENST00000621629.4:c.*501G>T
|
ENSP00000478747.1:n.*501G>T
|
|
NM_001130997.2:c.625G>T
|
NP_001124469.1:p.Ala209Ser
|
|
NM_152274.4:c.625G>T
|
NP_689487.2:p.Ala209Ser
|
|
XM_005277920.3:c.595G>T
|
XP_005277977.1:p.Ala199Ser
|
|
XM_005277921.3:c.595G>T
|
XP_005277978.1:p.Ala199Ser
|
|
XM_011531213.1:c.499G>T
|
XP_011529515.1:p.Ala167Ser
|
|
XM_011531214.1:c.499G>T
|
XP_011529516.1:p.Ala167Ser
|
|
XM_011531215.1:c.499G>T
|
XP_011529517.1:p.Ala167Ser
|
|
XM_005277920.4:c.595G>T
|
XP_005277977.1:p.Ala199Ser
|
|
XM_005277921.4:c.595G>T
|
XP_005277978.1:p.Ala199Ser
|
|
XM_011531214.2:c.499G>T
|
XP_011529516.1:p.Ala167Ser
|
|
XM_011531215.2:c.499G>T
|
XP_011529517.1:p.Ala167Ser
|
|
XR_002958810.1:n.2530G>T
|
|
|
NM_152274.5:c.625G>T
MANE Select
|
NP_689487.2:p.Ala209Ser
|
|
NM_001130997.3:c.625G>T
|
NP_001124469.1:p.Ala209Ser
|
|