ENST00000360319.9:c.6337G>T
|
ENSP00000353467.4:p.Ala2113Ser
|
|
ENST00000369850.10:c.6361G>T
MANE Select
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ENSP00000358866.3:p.Ala2121Ser
|
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ENST00000369856.8:c.6280G>T
|
ENSP00000358872.4:p.Ala2094Ser
|
|
ENST00000422373.6:c.3161-115G>T
|
ENSP00000416926.2:n.3161-115G>T
|
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ENST00000610817.5:c.6418G>T
|
ENSP00000480593.2:n.6418G>T
|
|
ENST00000673639.2:c.280-4100G>T
|
|
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ENST00000676696.1:c.6640G>T
|
ENSP00000503392.1:n.6640G>T
|
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ENST00000678304.1:n.1540G>T
|
|
|
ENST00000344736.8:c.6241G>T
|
ENSP00000358863.3:p.Ala2081Ser
|
|
ENST00000360319.8:c.6337G>T
|
ENSP00000353467.4:p.Ala2113Ser
|
|
ENST00000369850.7:c.6361G>T
|
ENSP00000358866.3:p.Ala2121Ser
|
|
ENST00000369856.7:c.6280G>T
|
ENSP00000358872.4:p.Ala2094Ser
|
|
ENST00000415241.1:c.563G>T
|
|
|
ENST00000420627.5:c.6317G>T
|
ENSP00000408921.1:n.6317G>T
|
|
ENST00000422373.5:c.6337G>T
|
ENSP00000416926.1:p.Ala2113Ser
|
|
ENST00000444578.1:c.304G>T
|
ENSP00000397824.1:p.Ala102Ser
|
|
ENST00000466325.1:n.576G>T
|
|
|
ENST00000490936.5:n.2350G>T
|
|
|
ENST00000498411.1:n.67+27G>T
|
|
|
ENST00000610817.4:c.5844+603G>T
|
ENSP00000480593.1:n.5844+603G>T
|
|
NM_001110556.1:c.6361G>T
|
NP_001104026.1:p.Ala2121Ser
|
|
NM_001456.3:c.6337G>T
|
NP_001447.2:p.Ala2113Ser
|
|
XM_011531127.1:c.6265G>T
|
XP_011529429.1:p.Ala2089Ser
|
|
XM_011531128.1:c.6241G>T
|
XP_011529430.1:p.Ala2081Ser
|
|
XM_011531129.1:c.6187G>T
|
XP_011529431.1:p.Ala2063Ser
|
|
XM_011531130.1:c.6163G>T
|
XP_011529432.1:p.Ala2055Ser
|
|
XM_011531131.1:c.6160G>T
|
XP_011529433.1:p.Ala2054Ser
|
|
NM_001110556.2:c.6361G>T
MANE Select
|
NP_001104026.1:p.Ala2121Ser
|
|
NM_001456.4:c.6337G>T
|
NP_001447.2:p.Ala2113Ser
|
|