ENST00000310018.7:c.1835T=
MANE Select
|
ENSP00000308122.2:p.Ile612=
|
|
ENST00000478480.2:c.1061T=
|
ENSP00000495261.1:p.Ile354=
|
|
ENST00000644341.1:c.1061T=
|
ENSP00000495642.1:p.Ile354=
|
|
ENST00000645515.1:c.1835T=
|
ENSP00000496421.1:p.Ile612=
|
|
ENST00000647427.1:c.728T=
|
ENSP00000496259.1:p.Ile243=
|
|
ENST00000310018.6:c.1835T=
|
ENSP00000308122.2:p.Ile612=
|
|
ENST00000353492.4:c.1835T=
|
ENSP00000253856.6:p.Ile612=
|
|
ENST00000393054.5:c.1835T=
|
ENSP00000376774.1:p.Ile612=
|
|
NM_020632.2:c.1835T=
|
NP_065683.2:p.Ile612=
|
|
NM_130840.2:c.1835T=
|
NP_570855.2:p.Ile612=
|
|
NM_130841.2:c.1835T=
|
NP_570856.2:p.Ile612=
|
|
XM_005250393.1:c.1835T=
|
XP_005250450.1:p.Ile612=
|
|
XM_005250394.2:c.1835T=
|
XP_005250451.1:p.Ile612=
|
|
XM_005250394.3:c.1835T=
|
XP_005250451.1:p.Ile612=
|
|
NM_020632.3:c.1835T=
MANE Select
|
NP_065683.2:p.Ile612=
|
|
NM_130840.3:c.1835T=
|
NP_570855.2:p.Ile612=
|
|
NM_130841.3:c.1835T=
|
NP_570856.2:p.Ile612=
|
|