ENST00000478003.2:n.1933C>G
|
|
|
ENST00000682276.1:n.1550C>G
|
|
|
ENST00000682892.1:c.1652C>G
|
ENSP00000507214.1:p.Pro551Arg
|
|
ENST00000682952.1:n.1744C>G
|
|
|
ENST00000684455.1:c.1318C>G
|
|
|
ENST00000684642.1:c.1502C>G
|
ENSP00000507355.1:p.Pro501Arg
|
|
ENST00000684740.1:n.2283C>G
|
|
|
ENST00000303236.9:c.2105C>G
MANE Select
|
ENSP00000307235.3:p.Pro702Arg
|
|
ENST00000652099.1:c.2299C>G
|
|
|
ENST00000652736.1:n.1981C>G
|
|
|
ENST00000303236.7:c.2105C>G
|
ENSP00000307235.3:p.Pro702Arg
|
|
ENST00000415570.1:c.1742C>G
|
ENSP00000412076.1:p.Pro581Arg
|
|
ENST00000419748.5:c.1652C>G
|
ENSP00000408325.1:p.Pro551Arg
|
|
ENST00000470706.1:n.31C>G
|
|
|
NM_001313915.1:c.1652C>G
|
NP_001300844.1:p.Pro551Arg
|
|
NM_004836.5:c.2105C>G
|
NP_004827.4:p.Pro702Arg
|
|
NM_004836.6:c.2105C>G
|
NP_004827.4:p.Pro702Arg
|
|
NR_110236.1:n.1515G>C
|
|
|
XM_005264649.3:c.1421C>G
|
XP_005264706.1:p.Pro474Arg
|
|
XR_939749.1:n.2384C>G
|
|
|
XM_017005376.2:c.1421C>G
|
XP_016860865.1:p.Pro474Arg
|
|
NM_004836.7:c.2105C>G
MANE Select
|
NP_004827.4:p.Pro702Arg
|
|
NM_001313915.2:c.1652C>G
|
NP_001300844.1:p.Pro551Arg
|
|