ENST00000376883.2:c.1366A=
MANE Select
|
ENSP00000366080.2:p.Met456=
|
|
ENST00000488757.6:c.1150A=
|
ENSP00000418259.2:p.Met384=
|
|
ENST00000376881.4:c.1114A=
|
ENSP00000366078.4:p.Met372=
|
|
ENST00000376883.1:c.1306A=
|
ENSP00000366080.1:p.Met436=
|
|
ENST00000488757.5:c.1366A=
|
ENSP00000418259.1:p.Met456=
|
|
NM_001109809.2:c.1366A=
|
NP_001103279.2:p.Met456=
|
|
XM_006715087.2:c.1150A=
|
XP_006715150.1:p.Met384=
|
|
XM_011514570.1:c.1366A=
|
XP_011512872.1:p.Met456=
|
|
NM_001109809.3:c.1366A=
|
NP_001103279.2:p.Met456=
|
|
NM_001366333.1:c.1150A=
|
NP_001353262.1:p.Met384=
|
|
NM_001109809.4:c.1366A=
|
NP_001103279.2:p.Met456=
|
|
NM_001366333.2:c.1150A=
|
NP_001353262.1:p.Met384=
|
|
NM_001109809.5:c.1366A=
MANE Select
|
NP_001103279.2:p.Met456=
|
|