ENST00000706989.1:c.2421C>G
|
ENSP00000516702.1:p.Ser807=
|
|
ENST00000359125.7:c.2367C>G
MANE Select
|
ENSP00000352035.2:p.Ser789=
|
|
ENST00000637193.1:c.1764C>G
|
ENSP00000490734.1:p.Ser588=
|
|
ENST00000344462.8:c.2274C>G
|
ENSP00000339611.4:p.Ser758=
|
|
ENST00000357249.6:c.1935C>G
|
ENSP00000349789.3:p.Ser645=
|
|
ENST00000359125.6:c.2367C>G
|
ENSP00000352035.2:p.Ser789=
|
|
ENST00000360480.7:c.2283C>G
|
ENSP00000353668.3:p.Ser761=
|
|
ENST00000370224.5:c.2241+150C>G
|
ENSP00000359244.2:n.2241+150C>G
|
|
ENST00000625514.2:c.2205+150C>G
|
ENSP00000486040.1:n.2205+150C>G
|
|
ENST00000626839.2:c.2313C>G
|
ENSP00000486706.1:p.Ser771=
|
|
ENST00000629241.2:c.2133+150C>G
|
ENSP00000487142.1:n.2133+150C>G
|
|
ENST00000629676.2:c.1680-6053C>G
|
ENSP00000486194.1:n.1680-6053C>G
|
|
NM_004518.4:c.2283C>G
|
NP_004509.2:p.Ser761=
|
|
NM_172106.1:c.2313C>G
|
NP_742104.1:p.Ser771=
|
|
NM_172107.2:c.2367C>G
|
NP_742105.1:p.Ser789=
|
|
NM_172108.3:c.2274C>G
|
NP_742106.1:p.Ser758=
|
|
XM_006723787.1:c.2409C>G
|
XP_006723850.1:p.Ser803=
|
|
XM_011528807.1:c.2475C>G
|
XP_011527109.1:p.Ser825=
|
|
XM_011528808.1:c.2472C>G
|
XP_011527110.1:p.Ser824=
|
|
XM_011528809.1:c.2445C>G
|
XP_011527111.1:p.Ser815=
|
|
XM_011528810.1:c.2421C>G
|
XP_011527112.1:p.Ser807=
|
|
XM_011528811.1:c.2391C>G
|
XP_011527113.1:p.Ser797=
|
|
XM_011528812.1:c.2364C>G
|
XP_011527114.1:p.Ser788=
|
|
XM_011528813.1:c.2349C>G
|
XP_011527115.1:p.Ser783=
|
|
XM_011528814.1:c.1956C>G
|
XP_011527116.1:p.Ser652=
|
|
NM_004518.5:c.2283C>G
|
NP_004509.2:p.Ser761=
|
|
NM_172106.2:c.2313C>G
|
NP_742104.1:p.Ser771=
|
|
NM_172107.3:c.2367C>G
|
NP_742105.1:p.Ser789=
|
|
NM_172108.4:c.2274C>G
|
NP_742106.1:p.Ser758=
|
|
XM_011528810.2:c.2421C>G
|
XP_011527112.1:p.Ser807=
|
|
XM_011528811.2:c.2391C>G
|
XP_011527113.1:p.Ser797=
|
|
XM_017027841.2:c.2418C>G
|
XP_016883330.1:p.Ser806=
|
|
XM_017027842.2:c.2355C>G
|
XP_016883331.1:p.Ser785=
|
|
XM_017027843.1:c.2352C>G
|
XP_016883332.1:p.Ser784=
|
|
XM_017027844.2:c.2310C>G
|
XP_016883333.1:p.Ser770=
|
|
XM_017027845.1:c.1383C>G
|
XP_016883334.1:p.Ser461=
|
|
NM_004518.6:c.2283C>G
|
NP_004509.2:p.Ser761=
|
|
NM_172106.3:c.2313C>G
|
NP_742104.1:p.Ser771=
|
|
NM_172107.4:c.2367C>G
MANE Select
|
NP_742105.1:p.Ser789=
|
|
NM_172108.5:c.2274C>G
|
NP_742106.1:p.Ser758=
|
|
NM_001382235.1:c.2421C>G
|
NP_001369164.1:p.Ser807=
|
|