|
ENST00000395796.8:c.*1266T>C
|
ENSP00000379142.4:n.*1266T>C
|
|
|
ENST00000616242.5:c.*388T>C
|
ENSP00000482149.2:n.*388T>C
|
|
|
ENST00000683378.1:n.494T>C
|
|
|
|
ENST00000336642.9:c.302T>C
|
ENSP00000338009.5:p.Phe101Ser
|
|
|
ENST00000345378.7:c.1271T>C
|
ENSP00000223366.2:p.Phe424Ser
|
|
|
ENST00000403799.8:c.1268T>C
MANE Select
|
ENSP00000384247.3:p.Phe423Ser
|
|
|
ENST00000671824.1:c.1331T>C
|
ENSP00000500264.1:p.Phe444Ser
|
|
|
ENST00000672743.1:n.280T>C
|
|
|
|
ENST00000673284.1:c.1268T>C
|
ENSP00000499852.1:p.Phe423Ser
|
|
|
ENST00000336642.8:c.320T>C
|
ENSP00000338009.4:p.Phe107Ser
|
|
|
ENST00000345378.6:c.1271T>C
|
ENSP00000223366.2:p.Phe424Ser
|
|
|
ENST00000395796.7:c.1265T>C
|
ENSP00000379142.3:p.Phe422Ser
|
|
|
ENST00000403799.7:c.1268T>C
|
ENSP00000384247.3:p.Phe423Ser
|
|
|
ENST00000437084.1:c.1217T>C
|
ENSP00000402840.1:p.Phe406Ser
|
|
|
ENST00000459642.1:n.648T>C
|
|
|
|
ENST00000616242.4:c.1265T>C
|
ENSP00000482149.1:p.Phe422Ser
|
|
|
NM_000162.3:c.1268T>C
|
NP_000153.1:p.Phe423Ser
|
|
|
NM_033507.1:c.1271T>C
|
NP_277042.1:p.Phe424Ser
|
|
|
NM_033508.1:c.1265T>C
|
NP_277043.1:p.Phe422Ser
|
|
|
NM_000162.4:c.1268T>C
|
NP_000153.1:p.Phe423Ser
|
|
|
NM_001354800.1:c.1268T>C
|
NP_001341729.1:p.Phe423Ser
|
|
|
NM_001354801.1:c.257T>C
|
NP_001341730.1:p.Phe86Ser
|
|
|
NM_001354802.1:c.128T>C
|
NP_001341731.1:p.Phe43Ser
|
|
|
NM_001354803.1:c.302T>C
|
NP_001341732.1:p.Phe101Ser
|
|
|
NM_033507.2:c.1271T>C
|
NP_277042.1:p.Phe424Ser
|
|
|
NM_033508.2:c.1265T>C
|
NP_277043.1:p.Phe422Ser
|
|
|
XM_024446707.1:c.128T>C
|
XP_024302475.1:p.Phe43Ser
|
|
|
NM_000162.5:c.1268T>C
MANE Select
|
NP_000153.1:p.Phe423Ser
|
|
|
NM_033507.3:c.1271T>C
|
NP_277042.1:p.Phe424Ser
|
|
|
NM_033508.3:c.1265T>C
|
NP_277043.1:p.Phe422Ser
|
|
|
NM_001354803.2:c.302T>C
|
NP_001341732.1:p.Phe101Ser
|
|
