ENST00000703118.1:c.*1277C>T
|
ENSP00000515181.1:n.*1277C>T
|
|
ENST00000703131.1:n.1706C>T
|
|
|
ENST00000703139.1:c.539C>T
|
|
|
ENST00000703140.1:c.5689C>T
|
ENSP00000515197.1:p.His1897Tyr
|
|
ENST00000703141.1:c.*1222C>T
|
ENSP00000515198.1:n.*1222C>T
|
|
ENST00000703142.1:c.*2732C>T
|
ENSP00000515199.1:n.*2732C>T
|
|
ENST00000361445.9:c.5902C>T
MANE Select
|
ENSP00000354558.4:p.His1968Tyr
|
|
ENST00000361445.8:c.5902C>T
|
ENSP00000354558.4:p.His1968Tyr
|
|
ENST00000376838.5:c.517C>T
|
ENSP00000366034.1:p.His173Tyr
|
|
NM_004958.3:c.5902C>T , LRG_734t1:c.5902C>T
|
NP_004949.1:p.His1968Tyr
|
|
XM_005263438.1:c.5902C>T
|
XP_005263495.1:p.His1968Tyr
|
|
XR_244786.1:n.6023C>T
|
|
|
XM_005263438.2:c.5902C>T
|
XP_005263495.1:p.His1968Tyr
|
|
XM_017000900.1:c.5221C>T
|
XP_016856389.1:p.His1741Tyr
|
|
XM_017000901.1:c.4654C>T
|
XP_016856390.1:p.His1552Tyr
|
|
XM_024446187.1:c.5902C>T
|
XP_024301955.1:p.His1968Tyr
|
|
XR_001737087.1:n.6023C>T
|
|
|
NM_004958.4:c.5902C>T
MANE Select
|
NP_004949.1:p.His1968Tyr
|
|
NM_001386500.1:c.5902C>T
|
NP_001373429.1:p.His1968Tyr
|
|
NM_001386501.1:c.4654C>T
|
NP_001373430.1:p.His1552Tyr
|
|