ENST00000342741.6:c.906T>A
MANE Select
|
ENSP00000339933.4:p.Gly302=
|
|
ENST00000342741.4:c.906T>A
|
ENSP00000339933.4:p.Gly302=
|
|
ENST00000392414.7:c.813T>A
|
ENSP00000376214.3:p.Gly271=
|
|
NM_000298.5:c.906T>A
|
NP_000289.1:p.Gly302=
|
|
NM_181871.3:c.813T>A
|
NP_870986.1:p.Gly271=
|
|
XM_005245266.3:c.1065T>A
|
XP_005245323.1:p.Gly355=
|
|
XM_006711386.2:c.714T>A
|
XP_006711449.1:p.Gly238=
|
|
XM_011509639.1:c.1065T>A
|
XP_011507941.1:p.Gly355=
|
|
XM_011509640.1:c.714T>A
|
XP_011507942.1:p.Gly238=
|
|
NM_000298.6:c.906T>A
MANE Select
|
NP_000289.1:p.Gly302=
|
|
XM_006711386.4:c.714T>A
|
XP_006711449.1:p.Gly238=
|
|
XM_011509640.3:c.714T>A
|
XP_011507942.1:p.Gly238=
|
|
XM_017001493.1:c.906T>A
|
XP_016856982.1:p.Gly302=
|
|
NM_181871.4:c.813T>A
|
NP_870986.1:p.Gly271=
|
|