ENST00000267845.8:c.1962C>G
MANE Select
|
ENSP00000267845.3:p.Pro654=
|
|
ENST00000267845.7:c.1962C>G
|
ENSP00000267845.3:p.Pro654=
|
|
ENST00000543581.5:c.1863C>G
|
ENSP00000440252.1:p.Pro621=
|
|
ENST00000559816.1:n.1706C>G
|
|
|
NM_001306146.1:c.1863C>G
|
NP_001293075.1:p.Pro621=
|
|
NM_002112.3:c.1962C>G
|
NP_002103.2:p.Pro654=
|
|
XM_011521479.1:c.1725C>G
|
XP_011519781.1:p.Pro575=
|
|
XM_011521480.1:c.1530C>G
|
XP_011519782.1:p.Pro510=
|
|
XM_017022094.1:c.2067C>G
|
XP_016877583.1:p.Pro689=
|
|
XM_017022095.1:c.1968C>G
|
XP_016877584.1:p.Pro656=
|
|
XM_017022096.1:c.1839C>G
|
XP_016877585.1:p.Pro613=
|
|
XM_017022097.1:c.1830C>G
|
XP_016877586.1:p.Pro610=
|
|
XM_017022098.1:c.1635C>G
|
XP_016877587.1:p.Pro545=
|
|
NM_002112.4:c.1962C>G
MANE Select
|
NP_002103.2:p.Pro654=
|
|
NM_001306146.2:c.1863C>G
|
NP_001293075.1:p.Pro621=
|
|