ENST00000270301.12:c.4244T>C
|
ENSP00000270301.6:p.Ile1415Thr
|
|
ENST00000401500.7:c.4259T>C
MANE Select
|
ENSP00000384792.1:p.Ile1420Thr
|
|
ENST00000587391.6:c.*4119T>C
|
ENSP00000465525.1:n.*4119T>C
|
|
ENST00000679357.1:c.2339T>C
|
|
|
ENST00000679598.1:c.1004T>C
|
|
|
ENST00000679682.1:c.4244T>C
|
ENSP00000506226.1:p.Ile1415Thr
|
|
ENST00000679714.1:c.4253T>C
|
ENSP00000506627.1:p.Ile1418Thr
|
|
ENST00000679757.1:c.3908T>C
|
ENSP00000505158.1:p.Ile1303Thr
|
|
ENST00000679858.1:c.*3641T>C
|
ENSP00000505655.1:n.*3641T>C
|
|
ENST00000680211.1:c.860T>C
|
ENSP00000506102.1:p.Ile287Thr
|
|
ENST00000680280.1:n.1762T>C
|
|
|
ENST00000680349.1:n.2908T>C
|
|
|
ENST00000680403.1:c.4244T>C
|
ENSP00000505677.1:p.Ile1415Thr
|
|
ENST00000680564.1:c.4010T>C
|
ENSP00000505582.1:p.Ile1337Thr
|
|
ENST00000680590.1:c.*2639T>C
|
ENSP00000505350.1:n.*2639T>C
|
|
ENST00000680597.1:c.992T>C
|
|
|
ENST00000680739.1:c.1274T>C
|
|
|
ENST00000680773.1:n.2760T>C
|
|
|
ENST00000680806.1:c.*3562T>C
|
ENSP00000506418.1:n.*3562T>C
|
|
ENST00000680997.1:n.2191T>C
|
|
|
ENST00000681608.1:n.2104T>C
|
|
|
ENST00000681625.1:c.*1591T>C
|
ENSP00000505555.1:n.*1591T>C
|
|
ENST00000681648.1:n.2310T>C
|
|
|
ENST00000270301.11:c.4244T>C
|
ENSP00000270301.6:p.Ile1415Thr
|
|
ENST00000401500.6:c.4259T>C
|
ENSP00000384792.1:p.Ile1420Thr
|
|
ENST00000587391.5:c.*4119T>C
|
ENSP00000465525.1:n.*4119T>C
|
|
NM_001083961.1:c.4259T>C
|
NP_001077430.1:p.Ile1420Thr
|
|
NM_173636.4:c.4244T>C
|
NP_775907.4:p.Ile1415Thr
|
|
XM_005258809.2:c.4148T>C
|
XP_005258866.1:p.Ile1383Thr
|
|
XM_011526837.1:c.4244T>C
|
XP_011525139.1:p.Ile1415Thr
|
|
XM_011526838.1:c.4010T>C
|
XP_011525140.1:p.Ile1337Thr
|
|
XM_011526839.1:c.3908T>C
|
XP_011525141.1:p.Ile1303Thr
|
|
XM_011526840.1:c.3251T>C
|
XP_011525142.1:p.Ile1084Thr
|
|
XM_011526841.1:c.2837T>C
|
XP_011525143.1:p.Ile946Thr
|
|
XM_011526842.1:c.2690T>C
|
XP_011525144.1:p.Ile897Thr
|
|
XM_011526843.1:c.2006T>C
|
XP_011525145.1:p.Ile669Thr
|
|
XM_011526844.1:c.2006T>C
|
XP_011525146.1:p.Ile669Thr
|
|
XM_011526840.2:c.3251T>C
|
XP_011525142.1:p.Ile1084Thr
|
|
XM_011526841.2:c.2837T>C
|
XP_011525143.1:p.Ile946Thr
|
|
XM_011526844.2:c.2006T>C
|
XP_011525146.1:p.Ile669Thr
|
|
XM_017026665.1:c.4259T>C
|
XP_016882154.1:p.Ile1420Thr
|
|
NM_001083961.2:c.4259T>C
MANE Select
|
NP_001077430.1:p.Ile1420Thr
|
|
NM_173636.5:c.4244T>C
|
NP_775907.4:p.Ile1415Thr
|
|