ENST00000609119.2:c.*3692G>T
|
ENSP00000499659.2:n.*3692G>T
|
|
ENST00000659194.3:c.12588G>T
|
ENSP00000499653.3:p.Met4196Ile
|
|
ENST00000660292.2:c.12621G>T
|
ENSP00000499787.2:p.Met4207Ile
|
|
ENST00000659194.2:c.4777G>T
|
|
|
ENST00000366574.7:c.12600G>T
MANE Select
|
ENSP00000355533.2:p.Met4200Ile
|
|
ENST00000659194.1:c.4777G>T
|
|
|
ENST00000660292.1:c.2653G>T
|
|
|
ENST00000360064.7:c.12552G>T
|
ENSP00000353174.7:p.Met4184Ile
|
|
ENST00000366574.6:c.12600G>T
|
ENSP00000355533.2:p.Met4200Ile
|
|
ENST00000609119.1:n.3795G>T
|
|
|
NM_001035.2:c.12600G>T
|
NP_001026.2:p.Met4200Ile
|
|
XM_006711802.2:c.12654G>T
|
XP_006711865.1:p.Met4218Ile
|
|
XM_006711803.2:c.12651G>T
|
XP_006711866.1:p.Met4217Ile
|
|
XM_006711804.2:c.12630G>T
|
XP_006711867.1:p.Met4210Ile
|
|
XM_006711805.2:c.12624G>T
|
XP_006711868.1:p.Met4208Ile
|
|
XM_006711806.2:c.12618G>T
|
XP_006711869.1:p.Met4206Ile
|
|
XM_006711807.2:c.12594G>T
|
XP_006711870.1:p.Met4198Ile
|
|
XM_006711808.2:c.12417G>T
|
XP_006711871.1:p.Met4139Ile
|
|
XM_006711810.2:c.12561G>T
|
XP_006711873.1:p.Met4187Ile
|
|
XM_006711802.3:c.12654G>T
|
XP_006711865.1:p.Met4218Ile
|
|
XM_006711803.3:c.12651G>T
|
XP_006711866.1:p.Met4217Ile
|
|
XM_006711804.3:c.12630G>T
|
XP_006711867.1:p.Met4210Ile
|
|
XM_006711805.3:c.12624G>T
|
XP_006711868.1:p.Met4208Ile
|
|
XM_006711806.3:c.12618G>T
|
XP_006711869.1:p.Met4206Ile
|
|
XM_006711807.3:c.12594G>T
|
XP_006711870.1:p.Met4198Ile
|
|
XM_006711808.3:c.12417G>T
|
XP_006711871.1:p.Met4139Ile
|
|
XM_006711810.3:c.12561G>T
|
XP_006711873.1:p.Met4187Ile
|
|
XM_017002028.1:c.12633G>T
|
XP_016857517.1:p.Met4211Ile
|
|
NM_001035.3:c.12600G>T
MANE Select
|
NP_001026.2:p.Met4200Ile
|
|