ENST00000303115.8:c.882A=
MANE Select
|
ENSP00000306157.3:p.Leu294=
|
|
ENST00000303115.7:c.882A=
|
ENSP00000306157.3:p.Leu294=
|
|
ENST00000505093.1:c.197A=
|
ENSP00000426069.1:p.Ter66=
|
|
ENST00000505875.1:n.180A=
|
|
|
ENST00000514217.5:c.*76A=
|
ENSP00000427688.1:n.*76A=
|
|
NM_002185.3:c.882A=
|
NP_002176.2:p.Leu294=
|
|
NR_120485.1:n.722A=
|
|
|
XM_005248299.2:c.788A=
|
XP_005248356.1:p.Ter263=
|
|
NM_002185.4:c.882A=
|
NP_002176.2:p.Leu294=
|
|
NR_120485.2:n.748A=
|
|
|
XM_005248299.4:c.788A=
|
XP_005248356.1:p.Ter263=
|
|
NM_002185.5:c.882A=
MANE Select
|
NP_002176.2:p.Leu294=
|
|
NR_120485.3:n.706A=
|
|
|