ENST00000706989.1:c.2504T>A
|
ENSP00000516702.1:p.Leu835His
|
|
ENST00000359125.7:c.2450T>A
MANE Select
|
ENSP00000352035.2:p.Leu817His
|
|
ENST00000637193.1:c.1847T>A
|
ENSP00000490734.1:p.Leu616His
|
|
ENST00000344462.8:c.2357T>A
|
ENSP00000339611.4:p.Leu786His
|
|
ENST00000357249.6:c.2018T>A
|
ENSP00000349789.3:p.Leu673His
|
|
ENST00000359125.6:c.2450T>A
|
ENSP00000352035.2:p.Leu817His
|
|
ENST00000360480.7:c.2366T>A
|
ENSP00000353668.3:p.Leu789His
|
|
ENST00000370224.5:c.2241+233T>A
|
ENSP00000359244.2:n.2241+233T>A
|
|
ENST00000625514.2:c.2205+233T>A
|
ENSP00000486040.1:n.2205+233T>A
|
|
ENST00000626839.2:c.2396T>A
|
ENSP00000486706.1:p.Leu799His
|
|
ENST00000629241.2:c.2133+233T>A
|
ENSP00000487142.1:n.2133+233T>A
|
|
ENST00000629676.2:c.1680-5970T>A
|
ENSP00000486194.1:n.1680-5970T>A
|
|
NM_004518.4:c.2366T>A
|
NP_004509.2:p.Leu789His
|
|
NM_172106.1:c.2396T>A
|
NP_742104.1:p.Leu799His
|
|
NM_172107.2:c.2450T>A
|
NP_742105.1:p.Leu817His
|
|
NM_172108.3:c.2357T>A
|
NP_742106.1:p.Leu786His
|
|
XM_006723787.1:c.2492T>A
|
XP_006723850.1:p.Leu831His
|
|
XM_011528807.1:c.2558T>A
|
XP_011527109.1:p.Leu853His
|
|
XM_011528808.1:c.2555T>A
|
XP_011527110.1:p.Leu852His
|
|
XM_011528809.1:c.2528T>A
|
XP_011527111.1:p.Leu843His
|
|
XM_011528810.1:c.2504T>A
|
XP_011527112.1:p.Leu835His
|
|
XM_011528811.1:c.2474T>A
|
XP_011527113.1:p.Leu825His
|
|
XM_011528812.1:c.2447T>A
|
XP_011527114.1:p.Leu816His
|
|
XM_011528813.1:c.2432T>A
|
XP_011527115.1:p.Leu811His
|
|
XM_011528814.1:c.2039T>A
|
XP_011527116.1:p.Leu680His
|
|
NM_004518.5:c.2366T>A
|
NP_004509.2:p.Leu789His
|
|
NM_172106.2:c.2396T>A
|
NP_742104.1:p.Leu799His
|
|
NM_172107.3:c.2450T>A
|
NP_742105.1:p.Leu817His
|
|
NM_172108.4:c.2357T>A
|
NP_742106.1:p.Leu786His
|
|
XM_011528810.2:c.2504T>A
|
XP_011527112.1:p.Leu835His
|
|
XM_011528811.2:c.2474T>A
|
XP_011527113.1:p.Leu825His
|
|
XM_017027841.2:c.2501T>A
|
XP_016883330.1:p.Leu834His
|
|
XM_017027842.2:c.2438T>A
|
XP_016883331.1:p.Leu813His
|
|
XM_017027843.1:c.2435T>A
|
XP_016883332.1:p.Leu812His
|
|
XM_017027844.2:c.2393T>A
|
XP_016883333.1:p.Leu798His
|
|
XM_017027845.1:c.1466T>A
|
XP_016883334.1:p.Leu489His
|
|
NM_004518.6:c.2366T>A
|
NP_004509.2:p.Leu789His
|
|
NM_172106.3:c.2396T>A
|
NP_742104.1:p.Leu799His
|
|
NM_172107.4:c.2450T>A
MANE Select
|
NP_742105.1:p.Leu817His
|
|
NM_172108.5:c.2357T>A
|
NP_742106.1:p.Leu786His
|
|
NM_001382235.1:c.2504T>A
|
NP_001369164.1:p.Leu835His
|
|