ENST00000478003.2:n.2193C>G
|
|
|
ENST00000682276.1:n.1810C>G
|
|
|
ENST00000682892.1:c.1912C>G
|
ENSP00000507214.1:p.Pro638Ala
|
|
ENST00000682952.1:n.2004C>G
|
|
|
ENST00000684455.1:c.1578C>G
|
|
|
ENST00000684642.1:c.1762C>G
|
ENSP00000507355.1:p.Pro588Ala
|
|
ENST00000684740.1:n.2543C>G
|
|
|
ENST00000303236.9:c.2365C>G
MANE Select
|
ENSP00000307235.3:p.Pro789Ala
|
|
ENST00000652099.1:c.2559C>G
|
|
|
ENST00000652736.1:n.2241C>G
|
|
|
ENST00000303236.7:c.2365C>G
|
ENSP00000307235.3:p.Pro789Ala
|
|
ENST00000415570.1:c.2002C>G
|
ENSP00000412076.1:p.Pro668Ala
|
|
ENST00000419748.5:c.1912C>G
|
ENSP00000408325.1:p.Pro638Ala
|
|
ENST00000470706.1:n.49-41C>G
|
|
|
NM_001313915.1:c.1912C>G
|
NP_001300844.1:p.Pro638Ala
|
|
NM_004836.5:c.2365C>G
|
NP_004827.4:p.Pro789Ala
|
|
NM_004836.6:c.2365C>G
|
NP_004827.4:p.Pro789Ala
|
|
NR_110236.1:n.1255G>C
|
|
|
XM_005264649.3:c.1681C>G
|
XP_005264706.1:p.Pro561Ala
|
|
XM_017005376.2:c.1681C>G
|
XP_016860865.1:p.Pro561Ala
|
|
NM_004836.7:c.2365C>G
MANE Select
|
NP_004827.4:p.Pro789Ala
|
|
NM_001313915.2:c.1912C>G
|
NP_001300844.1:p.Pro638Ala
|
|