ENST00000254108.12:c.892A>T
MANE Select
|
ENSP00000254108.8:p.Ile298Phe
|
|
ENST00000254108.11:c.892A>T
|
ENSP00000254108.7:p.Ile298Phe
|
|
ENST00000380244.7:c.889A>T
|
ENSP00000369594.3:p.Ile297Phe
|
|
ENST00000474990.5:n.186A>T
|
|
|
ENST00000487509.6:n.4067A>T
|
|
|
ENST00000564766.1:n.716A>T
|
|
|
ENST00000566605.5:c.*65A>T
|
ENSP00000455073.1:n.*65A>T
|
|
ENST00000568685.1:c.895A>T
|
ENSP00000455282.1:p.Ile299Phe
|
|
ENST00000568901.2:n.266A>T
|
|
|
NM_001170634.1:c.889A>T
|
NP_001164105.1:p.Ile297Phe
|
|
NM_001170937.1:c.880A>T
|
NP_001164408.1:p.Ile294Phe
|
|
NM_004960.3:c.892A>T , LRG_655t1:c.892A>T
|
NP_004951.1:p.Ile298Phe
|
|
NR_028388.2:n.962A>T
|
|
|
XM_005255233.3:c.277A>T
|
XP_005255290.1:p.Ile93Phe
|
|
XM_011545781.1:c.886A>T
|
XP_011544083.1:p.Ile296Phe
|
|
XM_011545782.1:c.277A>T
|
XP_011544084.1:p.Ile93Phe
|
|
XM_005255233.5:c.277A>T
|
XP_005255290.1:p.Ile93Phe
|
|
XM_011545782.2:c.277A>T
|
XP_011544084.1:p.Ile93Phe
|
|
XM_024450221.1:c.883A>T
|
XP_024305989.1:p.Ile295Phe
|
|
NM_004960.4:c.892A>T
MANE Select
|
NP_004951.1:p.Ile298Phe
|
|