ENST00000706989.1:c.2524G=
|
ENSP00000516702.1:p.Val842=
|
|
ENST00000359125.7:c.2470G=
MANE Select
|
ENSP00000352035.2:p.Val824=
|
|
ENST00000637193.1:c.1867G=
|
ENSP00000490734.1:p.Val623=
|
|
ENST00000344462.8:c.2377G=
|
ENSP00000339611.4:p.Val793=
|
|
ENST00000357249.6:c.2038G=
|
ENSP00000349789.3:p.Val680=
|
|
ENST00000359125.6:c.2470G=
|
ENSP00000352035.2:p.Val824=
|
|
ENST00000360480.7:c.2386G=
|
ENSP00000353668.3:p.Val796=
|
|
ENST00000370224.5:c.2241+253G=
|
ENSP00000359244.2:n.2241+253G=
|
|
ENST00000625514.2:c.2205+253G=
|
ENSP00000486040.1:n.2205+253G=
|
|
ENST00000626839.2:c.2416G=
|
ENSP00000486706.1:p.Val806=
|
|
ENST00000629241.2:c.2133+253G=
|
ENSP00000487142.1:n.2133+253G=
|
|
ENST00000629676.2:c.1680-5950G=
|
ENSP00000486194.1:n.1680-5950G=
|
|
NM_004518.4:c.2386G=
|
NP_004509.2:p.Val796=
|
|
NM_172106.1:c.2416G=
|
NP_742104.1:p.Val806=
|
|
NM_172107.2:c.2470G=
|
NP_742105.1:p.Val824=
|
|
NM_172108.3:c.2377G=
|
NP_742106.1:p.Val793=
|
|
XM_006723787.1:c.2512G=
|
XP_006723850.1:p.Val838=
|
|
XM_011528807.1:c.2578G=
|
XP_011527109.1:p.Val860=
|
|
XM_011528808.1:c.2575G=
|
XP_011527110.1:p.Val859=
|
|
XM_011528809.1:c.2548G=
|
XP_011527111.1:p.Val850=
|
|
XM_011528810.1:c.2524G=
|
XP_011527112.1:p.Val842=
|
|
XM_011528811.1:c.2494G=
|
XP_011527113.1:p.Val832=
|
|
XM_011528812.1:c.2467G=
|
XP_011527114.1:p.Val823=
|
|
XM_011528813.1:c.2452G=
|
XP_011527115.1:p.Val818=
|
|
XM_011528814.1:c.2059G=
|
XP_011527116.1:p.Val687=
|
|
NM_004518.5:c.2386G=
|
NP_004509.2:p.Val796=
|
|
NM_172106.2:c.2416G=
|
NP_742104.1:p.Val806=
|
|
NM_172107.3:c.2470G=
|
NP_742105.1:p.Val824=
|
|
NM_172108.4:c.2377G=
|
NP_742106.1:p.Val793=
|
|
XM_011528810.2:c.2524G=
|
XP_011527112.1:p.Val842=
|
|
XM_011528811.2:c.2494G=
|
XP_011527113.1:p.Val832=
|
|
XM_017027841.2:c.2521G=
|
XP_016883330.1:p.Val841=
|
|
XM_017027842.2:c.2458G=
|
XP_016883331.1:p.Val820=
|
|
XM_017027843.1:c.2455G=
|
XP_016883332.1:p.Val819=
|
|
XM_017027844.2:c.2413G=
|
XP_016883333.1:p.Val805=
|
|
XM_017027845.1:c.1486G=
|
XP_016883334.1:p.Val496=
|
|
NM_004518.6:c.2386G=
|
NP_004509.2:p.Val796=
|
|
NM_172106.3:c.2416G=
|
NP_742104.1:p.Val806=
|
|
NM_172107.4:c.2470G=
MANE Select
|
NP_742105.1:p.Val824=
|
|
NM_172108.5:c.2377G=
|
NP_742106.1:p.Val793=
|
|
NM_001382235.1:c.2524G=
|
NP_001369164.1:p.Val842=
|
|