ENST00000328300.11:c.3150T>A
MANE Select
|
ENSP00000331902.7:p.Pro1050=
|
|
ENST00000361603.7:c.3150T>A
|
ENSP00000354505.2:p.Pro1050=
|
|
ENST00000328300.10:c.3150T>A
|
ENSP00000331902.6:p.Pro1050=
|
|
ENST00000361603.6:c.3150T>A
|
ENSP00000354505.2:p.Pro1050=
|
|
ENST00000483338.1:n.2606T>A
|
|
|
ENST00000505728.1:c.383T>A
|
|
|
NM_000495.4:c.3150T>A
|
NP_000486.1:p.Pro1050=
|
|
NM_033380.2:c.3150T>A
|
NP_203699.1:p.Pro1050=
|
|
XM_005262070.2:c.3150T>A
|
XP_005262127.1:p.Pro1050=
|
|
XM_005262072.3:c.3150T>A
|
XP_005262129.1:p.Pro1050=
|
|
XM_006724616.2:c.3150T>A
|
XP_006724679.1:p.Pro1050=
|
|
XM_011530849.1:c.2826T>A
|
XP_011529151.1:p.Pro942=
|
|
XM_011530850.1:c.3150T>A
|
XP_011529152.1:p.Pro1050=
|
|
XM_011530851.1:c.723T>A
|
XP_011529153.1:p.Pro241=
|
|
XM_011530849.2:c.3165T>A
|
XP_011529151.2:p.Pro1055=
|
|
XM_017029259.2:c.3165T>A
|
XP_016884748.1:p.Pro1055=
|
|
XM_017029260.1:c.3165T>A
|
XP_016884749.1:p.Pro1055=
|
|
XM_017029261.1:c.3165T>A
|
XP_016884750.1:p.Pro1055=
|
|
XM_017029262.2:c.3165T>A
|
XP_016884751.1:p.Pro1055=
|
|
XM_017029263.2:c.1485T>A
|
XP_016884752.1:p.Pro495=
|
|
NM_000495.5:c.3150T>A
|
NP_000486.1:p.Pro1050=
|
|
NM_033380.3:c.3150T>A
MANE Select
|
NP_203699.1:p.Pro1050=
|
|