|
ENST00000707132.1:n.2114T>G
|
|
|
|
ENST00000707133.1:n.544T>G
|
|
|
|
ENST00000707134.1:n.813T>G
|
|
|
|
ENST00000346798.8:c.2147T>G
MANE Select
|
ENSP00000284981.4:p.Ile716Ser
|
|
|
ENST00000346798.7:c.2147T>G
|
ENSP00000284981.4:p.Ile716Ser
|
|
|
ENST00000348990.9:c.1922T>G
|
ENSP00000345463.5:p.Ile641Ser
|
|
|
ENST00000354192.7:c.1754T>G
|
ENSP00000346129.3:p.Ile585Ser
|
|
|
ENST00000357903.7:c.2090T>G
|
ENSP00000350578.3:p.Ile697Ser
|
|
|
ENST00000358918.7:c.2093T>G
|
ENSP00000351796.3:p.Ile698Ser
|
|
|
ENST00000359726.7:c.1817T>G
|
ENSP00000352760.4:p.Ile606Ser
|
|
|
ENST00000439274.6:c.1979T>G
|
ENSP00000398879.2:p.Ile660Ser
|
|
|
ENST00000440126.7:c.2075T>G
|
ENSP00000387483.2:p.Ile692Ser
|
|
|
ENST00000464867.1:n.494T>G
|
|
|
|
NM_000484.3:c.2147T>G
|
NP_000475.1:p.Ile716Ser
|
|
|
NM_001136016.3:c.2075T>G
|
NP_001129488.1:p.Ile692Ser
|
|
|
NM_001136129.2:c.1754T>G
|
NP_001129601.1:p.Ile585Ser
|
|
|
NM_001136130.2:c.1979T>G
|
NP_001129602.1:p.Ile660Ser
|
|
|
NM_001136131.2:c.1817T>G
|
NP_001129603.1:p.Ile606Ser
|
|
|
NM_001204301.1:c.2093T>G
|
NP_001191230.1:p.Ile698Ser
|
|
|
NM_001204302.1:c.2036T>G
|
NP_001191231.1:p.Ile679Ser
|
|
|
NM_001204303.1:c.1868T>G
|
NP_001191232.1:p.Ile623Ser
|
|
|
NM_201413.2:c.2090T>G
|
NP_958816.1:p.Ile697Ser
|
|
|
NM_201414.2:c.1922T>G
|
NP_958817.1:p.Ile641Ser
|
|
|
NM_000484.4:c.2147T>G
MANE Select
|
NP_000475.1:p.Ile716Ser
|
|
|
NM_001136129.3:c.1754T>G
|
NP_001129601.1:p.Ile585Ser
|
|
|
NM_001136130.3:c.1979T>G
|
NP_001129602.1:p.Ile660Ser
|
|
|
NM_001204301.2:c.2093T>G
|
NP_001191230.1:p.Ile698Ser
|
|
|
NM_001204302.2:c.2036T>G
|
NP_001191231.1:p.Ile679Ser
|
|
|
NM_001204303.2:c.1868T>G
|
NP_001191232.1:p.Ile623Ser
|
|
|
NM_201413.3:c.2090T>G
|
NP_958816.1:p.Ile697Ser
|
|
|
NM_201414.3:c.1922T>G
|
NP_958817.1:p.Ile641Ser
|
|
|
NM_001136131.3:c.1817T>G
|
NP_001129603.1:p.Ile606Ser
|
|
|
NM_001385253.1:c.1979T>G
|
NP_001372182.1:p.Ile660Ser
|
|
