ENST00000342741.6:c.1459T>C
MANE Select
|
ENSP00000339933.4:p.Tyr487His
|
|
ENST00000342741.4:c.1459T>C
|
ENSP00000339933.4:p.Tyr487His
|
|
ENST00000392414.7:c.1366T>C
|
ENSP00000376214.3:p.Tyr456His
|
|
NM_000298.5:c.1459T>C
|
NP_000289.1:p.Tyr487His
|
|
NM_181871.3:c.1366T>C
|
NP_870986.1:p.Tyr456His
|
|
XM_005245266.3:c.1618T>C
|
XP_005245323.1:p.Tyr540His
|
|
XM_006711386.2:c.1267T>C
|
XP_006711449.1:p.Tyr423His
|
|
XM_011509640.1:c.1267T>C
|
XP_011507942.1:p.Tyr423His
|
|
NM_000298.6:c.1459T>C
MANE Select
|
NP_000289.1:p.Tyr487His
|
|
XM_006711386.4:c.1267T>C
|
XP_006711449.1:p.Tyr423His
|
|
XM_011509640.3:c.1267T>C
|
XP_011507942.1:p.Tyr423His
|
|
NM_181871.4:c.1366T>C
|
NP_870986.1:p.Tyr456His
|
|