ENST00000355773.6:c.1314G>T
MANE Select
|
ENSP00000348019.5:p.Met438Ile
|
|
ENST00000355773.5:c.1314G>T
|
ENSP00000348019.5:p.Met438Ile
|
|
NM_012434.4:c.1314G>T
|
NP_036566.1:p.Met438Ile
|
|
XM_005248710.2:c.1263G>T
|
XP_005248767.1:p.Met421Ile
|
|
XM_005248711.1:c.1116G>T
|
XP_005248768.1:p.Met372Ile
|
|
XM_011535750.1:c.1166G>T
|
XP_011534052.1:p.Trp389Leu
|
|
NM_012434.5:c.1314G>T
MANE Select
|
NP_036566.1:p.Met438Ile
|
|
NM_001382629.1:c.1083G>T
|
NP_001369558.1:p.Met361Ile
|
|
NM_001382630.1:c.1260-5173G>T
|
NP_001369559.1:n.1260-5173G>T
|
|
NM_001382631.1:c.1335G>T
|
NP_001369560.1:p.Met445Ile
|
|
NM_001382632.1:c.1227G>T
|
NP_001369561.1:p.Met409Ile
|
|
NM_001382633.1:c.1314G>T
|
NP_001369562.1:p.Met438Ile
|
|
NM_001382634.1:c.1155G>T
|
NP_001369563.1:p.Met385Ile
|
|
NM_001382635.1:c.1311G>T
|
NP_001369564.1:p.Met437Ile
|
|
NM_001382636.1:c.996G>T
|
NP_001369565.1:p.Met332Ile
|
|