ENST00000355773.6:c.1115T>A
MANE Select
|
ENSP00000348019.5:p.Met372Lys
|
|
ENST00000355773.5:c.1115T>A
|
ENSP00000348019.5:p.Met372Lys
|
|
NM_012434.4:c.1115T>A
|
NP_036566.1:p.Met372Lys
|
|
XM_005248710.2:c.1064T>A
|
XP_005248767.1:p.Met355Lys
|
|
XM_005248711.1:c.917T>A
|
XP_005248768.1:p.Met306Lys
|
|
XM_011535750.1:c.1111+4771T>A
|
XP_011534052.1:n.1111+4771T>A
|
|
NM_012434.5:c.1115T>A
MANE Select
|
NP_036566.1:p.Met372Lys
|
|
NM_001382629.1:c.884T>A
|
NP_001369558.1:p.Met295Lys
|
|
NM_001382630.1:c.1115T>A
|
NP_001369559.1:p.Met372Lys
|
|
NM_001382631.1:c.1136T>A
|
NP_001369560.1:p.Met379Lys
|
|
NM_001382632.1:c.1028T>A
|
NP_001369561.1:p.Met343Lys
|
|
NM_001382633.1:c.1115T>A
|
NP_001369562.1:p.Met372Lys
|
|
NM_001382634.1:c.956T>A
|
NP_001369563.1:p.Met319Lys
|
|
NM_001382635.1:c.1112T>A
|
NP_001369564.1:p.Met371Lys
|
|
NM_001382636.1:c.797T>A
|
NP_001369565.1:p.Met266Lys
|
|