ENST00000371757.7:c.2260C>G
MANE Select
|
ENSP00000360822.2:p.Pro754Ala
|
|
ENST00000674572.1:c.2101C>G
|
ENSP00000501742.1:p.Pro701Ala
|
|
ENST00000675090.1:c.2008C>G
|
ENSP00000501833.1:p.Pro670Ala
|
|
ENST00000675399.1:c.2008C>G
|
ENSP00000501932.1:p.Pro670Ala
|
|
ENST00000676421.1:c.2017C>G
|
ENSP00000502322.1:p.Pro673Ala
|
|
ENST00000263604.5:c.2161C>G
|
ENSP00000263604.4:p.Pro721Ala
|
|
ENST00000371757.6:c.2260C>G
|
ENSP00000360822.2:p.Pro754Ala
|
|
ENST00000460750.5:c.*1870C>G
|
ENSP00000418777.1:n.*1870C>G
|
|
ENST00000486577.6:c.2143C>G
|
ENSP00000417578.3:p.Pro715Ala
|
|
ENST00000487664.5:c.2260C>G
|
ENSP00000417851.2:p.Pro754Ala
|
|
ENST00000488444.6:c.2203C>G
|
ENSP00000419007.3:p.Pro735Ala
|
|
ENST00000490355.6:c.2197C>G
|
ENSP00000418003.3:p.Pro733Ala
|
|
ENST00000490363.3:n.2079C>G
|
|
|
ENST00000491806.6:c.2203C>G
|
ENSP00000419086.3:p.Pro735Ala
|
|
ENST00000628528.2:c.2125C>G
|
ENSP00000486374.1:p.Pro709Ala
|
|
ENST00000630792.2:c.2095C>G
|
ENSP00000486486.1:p.Pro699Ala
|
|
ENST00000631073.2:c.2203C>G
|
ENSP00000486130.1:p.Pro735Ala
|
|
ENST00000631193.1:c.109C>G
|
ENSP00000486830.1:p.Pro37Ala
|
|
NM_001272003.1:c.2125C>G
|
NP_001258932.1:p.Pro709Ala
|
|
NM_020822.2:c.2260C>G
|
NP_065873.2:p.Pro754Ala
|
|
XM_011518877.1:c.2395C>G
|
XP_011517179.1:p.Pro799Ala
|
|
XM_011518878.1:c.2404C>G
|
XP_011517180.1:p.Pro802Ala
|
|
XM_011518879.1:c.2395C>G
|
XP_011517181.1:p.Pro799Ala
|
|
XM_011518880.1:c.2161C>G
|
XP_011517182.1:p.Pro721Ala
|
|
XM_011518881.1:c.1750C>G
|
XP_011517183.1:p.Pro584Ala
|
|
XM_011518877.3:c.2395C>G
|
XP_011517179.1:p.Pro799Ala
|
|
XM_011518878.3:c.2404C>G
|
XP_011517180.1:p.Pro802Ala
|
|
XM_011518879.3:c.2395C>G
|
XP_011517181.1:p.Pro799Ala
|
|
XM_011518881.3:c.1750C>G
|
XP_011517183.1:p.Pro584Ala
|
|
XM_017014931.1:c.2194C>G
|
XP_016870420.1:p.Pro732Ala
|
|
XM_017014932.1:c.2017C>G
|
XP_016870421.1:p.Pro673Ala
|
|
XM_017014933.1:c.1750C>G
|
XP_016870422.1:p.Pro584Ala
|
|
XM_024447617.1:c.1750C>G
|
XP_024303385.1:p.Pro584Ala
|
|
XM_024447618.1:c.1750C>G
|
XP_024303386.1:p.Pro584Ala
|
|
NM_020822.3:c.2260C>G
MANE Select
|
NP_065873.2:p.Pro754Ala
|
|
NM_001272003.2:c.2125C>G
|
NP_001258932.1:p.Pro709Ala
|
|