ENST00000324001.8:c.3442C>T
MANE Select
|
ENSP00000326018.6:p.Leu1148=
|
|
ENST00000673881.1:c.3025C>T
|
ENSP00000501070.1:p.Leu1009=
|
|
ENST00000674005.2:c.3727C>T
|
ENSP00000501261.1:p.Leu1243=
|
|
ENST00000674773.1:c.3025C>T
|
ENSP00000502579.1:p.Leu1009=
|
|
ENST00000675517.1:c.3317C>T
|
|
|
ENST00000676076.1:c.3303C>T
|
|
|
ENST00000676260.1:c.3404C>T
|
|
|
ENST00000676316.1:c.3329C>T
|
|
|
ENST00000291825.11:c.*3647C>T
|
ENSP00000291825.6:n.*3647C>T
|
|
ENST00000324001.7:c.3442C>T
|
ENSP00000326018.6:p.Leu1148=
|
|
NM_020956.2:c.*3647C>T , LRG_265t1:c.*3647C>T
|
NP_066007.1:n.*3647C>T
|
|
NM_181882.2:c.3442C>T , LRG_265t2:c.3442C>T
|
NP_870998.2:p.Leu1148=
|
|
XM_011527171.1:c.3442C>T
|
XP_011525473.1:p.Leu1148=
|
|
XM_011527171.2:c.3442C>T
|
XP_011525473.1:p.Leu1148=
|
|
XM_017027046.1:c.3340C>T
|
XP_016882535.1:p.Leu1114=
|
|
XM_017027047.1:c.3340C>T
|
XP_016882536.1:p.Leu1114=
|
|
NM_181882.3:c.3442C>T
MANE Select
|
NP_870998.2:p.Leu1148=
|
|