ENST00000706989.1:c.2173G>T
|
ENSP00000516702.1:p.Ala725Ser
|
|
ENST00000359125.7:c.2119G>T
MANE Select
|
ENSP00000352035.2:p.Ala707Ser
|
|
ENST00000637193.1:c.1516G>T
|
ENSP00000490734.1:p.Ala506Ser
|
|
ENST00000344462.8:c.2026G>T
|
ENSP00000339611.4:p.Ala676Ser
|
|
ENST00000357249.6:c.1687G>T
|
ENSP00000349789.3:p.Ala563Ser
|
|
ENST00000359125.6:c.2119G>T
|
ENSP00000352035.2:p.Ala707Ser
|
|
ENST00000360480.7:c.2035G>T
|
ENSP00000353668.3:p.Ala679Ser
|
|
ENST00000370224.5:c.2143G>T
|
ENSP00000359244.2:p.Ala715Ser
|
|
ENST00000625514.2:c.2107G>T
|
ENSP00000486040.1:p.Ala703Ser
|
|
ENST00000626839.2:c.2065G>T
|
ENSP00000486706.1:p.Ala689Ser
|
|
ENST00000629241.2:c.2035G>T
|
ENSP00000487142.1:p.Ala679Ser
|
|
ENST00000629676.2:c.1680-6301G>T
|
ENSP00000486194.1:n.1680-6301G>T
|
|
NM_004518.4:c.2035G>T
|
NP_004509.2:p.Ala679Ser
|
|
NM_172106.1:c.2065G>T
|
NP_742104.1:p.Ala689Ser
|
|
NM_172107.2:c.2119G>T
|
NP_742105.1:p.Ala707Ser
|
|
NM_172108.3:c.2026G>T
|
NP_742106.1:p.Ala676Ser
|
|
XM_006723787.1:c.2161G>T
|
XP_006723850.1:p.Ala721Ser
|
|
XM_011528807.1:c.2227G>T
|
XP_011527109.1:p.Ala743Ser
|
|
XM_011528808.1:c.2224G>T
|
XP_011527110.1:p.Ala742Ser
|
|
XM_011528809.1:c.2197G>T
|
XP_011527111.1:p.Ala733Ser
|
|
XM_011528810.1:c.2173G>T
|
XP_011527112.1:p.Ala725Ser
|
|
XM_011528811.1:c.2143G>T
|
XP_011527113.1:p.Ala715Ser
|
|
XM_011528812.1:c.2116G>T
|
XP_011527114.1:p.Ala706Ser
|
|
XM_011528813.1:c.2101G>T
|
XP_011527115.1:p.Ala701Ser
|
|
XM_011528814.1:c.1708G>T
|
XP_011527116.1:p.Ala570Ser
|
|
NM_004518.5:c.2035G>T
|
NP_004509.2:p.Ala679Ser
|
|
NM_172106.2:c.2065G>T
|
NP_742104.1:p.Ala689Ser
|
|
NM_172107.3:c.2119G>T
|
NP_742105.1:p.Ala707Ser
|
|
NM_172108.4:c.2026G>T
|
NP_742106.1:p.Ala676Ser
|
|
XM_011528810.2:c.2173G>T
|
XP_011527112.1:p.Ala725Ser
|
|
XM_011528811.2:c.2143G>T
|
XP_011527113.1:p.Ala715Ser
|
|
XM_017027841.2:c.2170G>T
|
XP_016883330.1:p.Ala724Ser
|
|
XM_017027842.2:c.2107G>T
|
XP_016883331.1:p.Ala703Ser
|
|
XM_017027843.1:c.2104G>T
|
XP_016883332.1:p.Ala702Ser
|
|
XM_017027844.2:c.2062G>T
|
XP_016883333.1:p.Ala688Ser
|
|
XM_017027845.1:c.1135G>T
|
XP_016883334.1:p.Ala379Ser
|
|
NM_004518.6:c.2035G>T
|
NP_004509.2:p.Ala679Ser
|
|
NM_172106.3:c.2065G>T
|
NP_742104.1:p.Ala689Ser
|
|
NM_172107.4:c.2119G>T
MANE Select
|
NP_742105.1:p.Ala707Ser
|
|
NM_172108.5:c.2026G>T
|
NP_742106.1:p.Ala676Ser
|
|
NM_001382235.1:c.2173G>T
|
NP_001369164.1:p.Ala725Ser
|
|