ENST00000706989.1:c.2316C>T
|
ENSP00000516702.1:p.Ala772=
|
|
ENST00000359125.7:c.2262C>T
MANE Select
|
ENSP00000352035.2:p.Ala754=
|
|
ENST00000637193.1:c.1659C>T
|
ENSP00000490734.1:p.Ala553=
|
|
ENST00000344462.8:c.2169C>T
|
ENSP00000339611.4:p.Ala723=
|
|
ENST00000357249.6:c.1830C>T
|
ENSP00000349789.3:p.Ala610=
|
|
ENST00000359125.6:c.2262C>T
|
ENSP00000352035.2:p.Ala754=
|
|
ENST00000360480.7:c.2178C>T
|
ENSP00000353668.3:p.Ala726=
|
|
ENST00000370224.5:c.2241+45C>T
|
ENSP00000359244.2:n.2241+45C>T
|
|
ENST00000625514.2:c.2205+45C>T
|
ENSP00000486040.1:n.2205+45C>T
|
|
ENST00000626839.2:c.2208C>T
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ENSP00000486706.1:p.Ala736=
|
|
ENST00000629241.2:c.2133+45C>T
|
ENSP00000487142.1:n.2133+45C>T
|
|
ENST00000629676.2:c.1680-6158C>T
|
ENSP00000486194.1:n.1680-6158C>T
|
|
NM_004518.4:c.2178C>T
|
NP_004509.2:p.Ala726=
|
|
NM_172106.1:c.2208C>T
|
NP_742104.1:p.Ala736=
|
|
NM_172107.2:c.2262C>T
|
NP_742105.1:p.Ala754=
|
|
NM_172108.3:c.2169C>T
|
NP_742106.1:p.Ala723=
|
|
XM_006723787.1:c.2304C>T
|
XP_006723850.1:p.Ala768=
|
|
XM_011528807.1:c.2370C>T
|
XP_011527109.1:p.Ala790=
|
|
XM_011528808.1:c.2367C>T
|
XP_011527110.1:p.Ala789=
|
|
XM_011528809.1:c.2340C>T
|
XP_011527111.1:p.Ala780=
|
|
XM_011528810.1:c.2316C>T
|
XP_011527112.1:p.Ala772=
|
|
XM_011528811.1:c.2286C>T
|
XP_011527113.1:p.Ala762=
|
|
XM_011528812.1:c.2259C>T
|
XP_011527114.1:p.Ala753=
|
|
XM_011528813.1:c.2244C>T
|
XP_011527115.1:p.Ala748=
|
|
XM_011528814.1:c.1851C>T
|
XP_011527116.1:p.Ala617=
|
|
NM_004518.5:c.2178C>T
|
NP_004509.2:p.Ala726=
|
|
NM_172106.2:c.2208C>T
|
NP_742104.1:p.Ala736=
|
|
NM_172107.3:c.2262C>T
|
NP_742105.1:p.Ala754=
|
|
NM_172108.4:c.2169C>T
|
NP_742106.1:p.Ala723=
|
|
XM_011528810.2:c.2316C>T
|
XP_011527112.1:p.Ala772=
|
|
XM_011528811.2:c.2286C>T
|
XP_011527113.1:p.Ala762=
|
|
XM_017027841.2:c.2313C>T
|
XP_016883330.1:p.Ala771=
|
|
XM_017027842.2:c.2250C>T
|
XP_016883331.1:p.Ala750=
|
|
XM_017027843.1:c.2247C>T
|
XP_016883332.1:p.Ala749=
|
|
XM_017027844.2:c.2205C>T
|
XP_016883333.1:p.Ala735=
|
|
XM_017027845.1:c.1278C>T
|
XP_016883334.1:p.Ala426=
|
|
NM_004518.6:c.2178C>T
|
NP_004509.2:p.Ala726=
|
|
NM_172106.3:c.2208C>T
|
NP_742104.1:p.Ala736=
|
|
NM_172107.4:c.2262C>T
MANE Select
|
NP_742105.1:p.Ala754=
|
|
NM_172108.5:c.2169C>T
|
NP_742106.1:p.Ala723=
|
|
NM_001382235.1:c.2316C>T
|
NP_001369164.1:p.Ala772=
|
|