|
ENST00000704289.1:c.*1356C>G
|
ENSP00000515816.1:n.*1356C>G
|
|
|
ENST00000315285.9:c.1696C>G
MANE Select
|
ENSP00000320885.3:p.Pro566Ala
|
|
|
ENST00000621856.2:c.1693C>G
|
ENSP00000482496.2:p.Pro565Ala
|
|
|
ENST00000642281.1:c.1433C>G
|
|
|
|
ENST00000642455.1:c.1597C>G
|
ENSP00000493827.1:p.Pro533Ala
|
|
|
ENST00000642751.1:c.1399C>G
|
|
|
|
ENST00000642999.1:c.1438C>G
|
ENSP00000496589.1:p.Pro480Ala
|
|
|
ENST00000643334.1:c.1276C>G
|
|
|
|
ENST00000644408.1:c.1595C>G
|
|
|
|
ENST00000644954.1:c.1342C>G
|
ENSP00000494312.1:p.Pro448Ala
|
|
|
ENST00000645159.1:n.2433C>G
|
|
|
|
ENST00000645671.1:c.1075C>G
|
|
|
|
ENST00000645730.1:c.875C>G
|
|
|
|
ENST00000646082.1:c.1342C>G
|
|
|
|
ENST00000646571.1:c.1600C>G
|
ENSP00000495015.1:p.Pro534Ala
|
|
|
ENST00000647007.1:n.1388C>G
|
|
|
|
ENST00000647133.1:c.1196C>G
|
|
|
|
ENST00000315285.7:c.1696C>G
|
ENSP00000320885.3:p.Pro566Ala
|
|
|
ENST00000345662.5:c.1600C>G
|
ENSP00000340817.1:p.Pro534Ala
|
|
|
ENST00000615843.4:c.1696C>G
|
ENSP00000480893.1:p.Pro566Ala
|
|
|
ENST00000621856.1:c.1438C>G
|
ENSP00000482496.1:p.Pro480Ala
|
|
|
NM_014946.3:c.1696C>G , LRG_714t1:c.1696C>G
|
NP_055761.2:p.Pro566Ala
|
|
|
NM_199436.1:c.1600C>G
|
NP_955468.1:p.Pro534Ala
|
|
|
XM_005264516.3:c.1693C>G
|
XP_005264573.1:p.Pro565Ala
|
|
|
XM_011533067.1:c.1625C>G
|
XP_011531369.1:p.Thr542Ser
|
|
|
NM_001363823.1:c.1693C>G
|
NP_001350752.1:p.Pro565Ala
|
|
|
NM_001363875.1:c.1597C>G
|
NP_001350804.1:p.Pro533Ala
|
|
|
XM_005264516.5:c.1693C>G
|
XP_005264573.1:p.Pro565Ala
|
|
|
XM_011533067.2:c.1625C>G
|
XP_011531369.1:p.Thr542Ser
|
|
|
XM_017004778.2:c.1529C>G
|
XP_016860267.1:p.Thr510Ser
|
|
|
NM_001363823.2:c.1693C>G
|
NP_001350752.1:p.Pro565Ala
|
|
|
NM_001363875.2:c.1597C>G
|
NP_001350804.1:p.Pro533Ala
|
|
|
NM_001377959.1:c.1529C>G
|
NP_001364888.1:p.Thr510Ser
|
|
|
NM_014946.4:c.1696C>G
MANE Select
|
NP_055761.2:p.Pro566Ala
|
|
|
NM_199436.2:c.1600C>G
|
NP_955468.1:p.Pro534Ala
|
|
