ENST00000254108.12:c.859A>T
MANE Select
|
ENSP00000254108.8:p.Ile287Phe
|
|
ENST00000254108.11:c.859A>T
|
ENSP00000254108.7:p.Ile287Phe
|
|
ENST00000380244.7:c.856A>T
|
ENSP00000369594.3:p.Ile286Phe
|
|
ENST00000474990.5:n.153A>T
|
|
|
ENST00000487509.6:n.4034A>T
|
|
|
ENST00000564766.1:n.683A>T
|
|
|
ENST00000566605.5:c.*32A>T
|
ENSP00000455073.1:n.*32A>T
|
|
ENST00000568685.1:c.862A>T
|
ENSP00000455282.1:p.Ile288Phe
|
|
ENST00000568901.2:n.233A>T
|
|
|
NM_001170634.1:c.856A>T
|
NP_001164105.1:p.Ile286Phe
|
|
NM_001170937.1:c.847A>T
|
NP_001164408.1:p.Ile283Phe
|
|
NM_004960.3:c.859A>T , LRG_655t1:c.859A>T
|
NP_004951.1:p.Ile287Phe
|
|
NR_028388.2:n.929A>T
|
|
|
XM_005255233.3:c.244A>T
|
XP_005255290.1:p.Ile82Phe
|
|
XM_011545781.1:c.853A>T
|
XP_011544083.1:p.Ile285Phe
|
|
XM_011545782.1:c.244A>T
|
XP_011544084.1:p.Ile82Phe
|
|
XM_005255233.5:c.244A>T
|
XP_005255290.1:p.Ile82Phe
|
|
XM_011545782.2:c.244A>T
|
XP_011544084.1:p.Ile82Phe
|
|
XM_024450221.1:c.850A>T
|
XP_024305989.1:p.Ile284Phe
|
|
NM_004960.4:c.859A>T
MANE Select
|
NP_004951.1:p.Ile287Phe
|
|