ENST00000267845.8:c.1795C>G
MANE Select
|
ENSP00000267845.3:p.Pro599Ala
|
|
ENST00000267845.7:c.1795C>G
|
ENSP00000267845.3:p.Pro599Ala
|
|
ENST00000543581.5:c.1696C>G
|
ENSP00000440252.1:p.Pro566Ala
|
|
ENST00000559816.1:n.1539C>G
|
|
|
NM_001306146.1:c.1696C>G
|
NP_001293075.1:p.Pro566Ala
|
|
NM_002112.3:c.1795C>G
|
NP_002103.2:p.Pro599Ala
|
|
XM_011521479.1:c.1558C>G
|
XP_011519781.1:p.Pro520Ala
|
|
XM_011521480.1:c.1363C>G
|
XP_011519782.1:p.Pro455Ala
|
|
XM_017022094.1:c.1900C>G
|
XP_016877583.1:p.Pro634Ala
|
|
XM_017022095.1:c.1801C>G
|
XP_016877584.1:p.Pro601Ala
|
|
XM_017022096.1:c.1672C>G
|
XP_016877585.1:p.Pro558Ala
|
|
XM_017022097.1:c.1663C>G
|
XP_016877586.1:p.Pro555Ala
|
|
XM_017022098.1:c.1468C>G
|
XP_016877587.1:p.Pro490Ala
|
|
NM_002112.4:c.1795C>G
MANE Select
|
NP_002103.2:p.Pro599Ala
|
|
NM_001306146.2:c.1696C>G
|
NP_001293075.1:p.Pro566Ala
|
|