|
ENST00000707132.1:n.2122A>G
|
|
|
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ENST00000707133.1:n.552A>G
|
|
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ENST00000707134.1:n.821A>G
|
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|
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ENST00000346798.8:c.2155A>G
MANE Select
|
ENSP00000284981.4:p.Thr719Ala
|
|
|
ENST00000346798.7:c.2155A>G
|
ENSP00000284981.4:p.Thr719Ala
|
|
|
ENST00000348990.9:c.1930A>G
|
ENSP00000345463.5:p.Thr644Ala
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|
|
ENST00000354192.7:c.1762A>G
|
ENSP00000346129.3:p.Thr588Ala
|
|
|
ENST00000357903.7:c.2098A>G
|
ENSP00000350578.3:p.Thr700Ala
|
|
|
ENST00000358918.7:c.2101A>G
|
ENSP00000351796.3:p.Thr701Ala
|
|
|
ENST00000359726.7:c.1825A>G
|
ENSP00000352760.4:p.Thr609Ala
|
|
|
ENST00000439274.6:c.1987A>G
|
ENSP00000398879.2:p.Thr663Ala
|
|
|
ENST00000440126.7:c.2083A>G
|
ENSP00000387483.2:p.Thr695Ala
|
|
|
ENST00000464867.1:n.502A>G
|
|
|
|
NM_000484.3:c.2155A>G
|
NP_000475.1:p.Thr719Ala
|
|
|
NM_001136016.3:c.2083A>G
|
NP_001129488.1:p.Thr695Ala
|
|
|
NM_001136129.2:c.1762A>G
|
NP_001129601.1:p.Thr588Ala
|
|
|
NM_001136130.2:c.1987A>G
|
NP_001129602.1:p.Thr663Ala
|
|
|
NM_001136131.2:c.1825A>G
|
NP_001129603.1:p.Thr609Ala
|
|
|
NM_001204301.1:c.2101A>G
|
NP_001191230.1:p.Thr701Ala
|
|
|
NM_001204302.1:c.2044A>G
|
NP_001191231.1:p.Thr682Ala
|
|
|
NM_001204303.1:c.1876A>G
|
NP_001191232.1:p.Thr626Ala
|
|
|
NM_201413.2:c.2098A>G
|
NP_958816.1:p.Thr700Ala
|
|
|
NM_201414.2:c.1930A>G
|
NP_958817.1:p.Thr644Ala
|
|
|
NM_000484.4:c.2155A>G
MANE Select
|
NP_000475.1:p.Thr719Ala
|
|
|
NM_001136129.3:c.1762A>G
|
NP_001129601.1:p.Thr588Ala
|
|
|
NM_001136130.3:c.1987A>G
|
NP_001129602.1:p.Thr663Ala
|
|
|
NM_001204301.2:c.2101A>G
|
NP_001191230.1:p.Thr701Ala
|
|
|
NM_001204302.2:c.2044A>G
|
NP_001191231.1:p.Thr682Ala
|
|
|
NM_001204303.2:c.1876A>G
|
NP_001191232.1:p.Thr626Ala
|
|
|
NM_201413.3:c.2098A>G
|
NP_958816.1:p.Thr700Ala
|
|
|
NM_201414.3:c.1930A>G
|
NP_958817.1:p.Thr644Ala
|
|
|
NM_001136131.3:c.1825A>G
|
NP_001129603.1:p.Thr609Ala
|
|
|
NM_001385253.1:c.1987A>G
|
NP_001372182.1:p.Thr663Ala
|
|
