ENST00000254108.12:c.894T>C
MANE Select
|
ENSP00000254108.8:p.Ile298=
|
|
ENST00000254108.11:c.894T>C
|
ENSP00000254108.7:p.Ile298=
|
|
ENST00000380244.7:c.891T>C
|
ENSP00000369594.3:p.Ile297=
|
|
ENST00000474990.5:n.188T>C
|
|
|
ENST00000487509.6:n.4069T>C
|
|
|
ENST00000564766.1:n.718T>C
|
|
|
ENST00000566605.5:c.*67T>C
|
ENSP00000455073.1:n.*67T>C
|
|
ENST00000568685.1:c.897T>C
|
ENSP00000455282.1:p.Ile299=
|
|
ENST00000568901.2:n.268T>C
|
|
|
NM_001170634.1:c.891T>C
|
NP_001164105.1:p.Ile297=
|
|
NM_001170937.1:c.882T>C
|
NP_001164408.1:p.Ile294=
|
|
NM_004960.3:c.894T>C , LRG_655t1:c.894T>C
|
NP_004951.1:p.Ile298=
|
|
NR_028388.2:n.964T>C
|
|
|
XM_005255233.3:c.279T>C
|
XP_005255290.1:p.Ile93=
|
|
XM_011545781.1:c.888T>C
|
XP_011544083.1:p.Ile296=
|
|
XM_011545782.1:c.279T>C
|
XP_011544084.1:p.Ile93=
|
|
XM_005255233.5:c.279T>C
|
XP_005255290.1:p.Ile93=
|
|
XM_011545782.2:c.279T>C
|
XP_011544084.1:p.Ile93=
|
|
XM_024450221.1:c.885T>C
|
XP_024305989.1:p.Ile295=
|
|
NM_004960.4:c.894T>C
MANE Select
|
NP_004951.1:p.Ile298=
|
|