ENST00000478003.2:n.1877A>T
|
|
|
ENST00000682276.1:n.1494A>T
|
|
|
ENST00000682892.1:c.1596A>T
|
ENSP00000507214.1:p.Pro532=
|
|
ENST00000682952.1:n.1688A>T
|
|
|
ENST00000684455.1:c.1262A>T
|
|
|
ENST00000684642.1:c.1446A>T
|
ENSP00000507355.1:p.Pro482=
|
|
ENST00000684740.1:n.2227A>T
|
|
|
ENST00000303236.9:c.2049A>T
MANE Select
|
ENSP00000307235.3:p.Pro683=
|
|
ENST00000652099.1:c.2243A>T
|
|
|
ENST00000652736.1:n.1925A>T
|
|
|
ENST00000303236.7:c.2049A>T
|
ENSP00000307235.3:p.Pro683=
|
|
ENST00000415570.1:c.1686A>T
|
ENSP00000412076.1:p.Pro562=
|
|
ENST00000419748.5:c.1596A>T
|
ENSP00000408325.1:p.Pro532=
|
|
ENST00000478003.1:n.615A>T
|
|
|
NM_001313915.1:c.1596A>T
|
NP_001300844.1:p.Pro532=
|
|
NM_004836.5:c.2049A>T
|
NP_004827.4:p.Pro683=
|
|
NM_004836.6:c.2049A>T
|
NP_004827.4:p.Pro683=
|
|
NR_110236.1:n.1571T>A
|
|
|
XM_005264649.3:c.1365A>T
|
XP_005264706.1:p.Pro455=
|
|
XR_939749.1:n.2328A>T
|
|
|
XM_017005376.2:c.1365A>T
|
XP_016860865.1:p.Pro455=
|
|
NM_004836.7:c.2049A>T
MANE Select
|
NP_004827.4:p.Pro683=
|
|
NM_001313915.2:c.1596A>T
|
NP_001300844.1:p.Pro532=
|
|