ENST00000706989.1:c.2528C>A
|
ENSP00000516702.1:p.Ala843Glu
|
|
ENST00000359125.7:c.2474C>A
MANE Select
|
ENSP00000352035.2:p.Ala825Glu
|
|
ENST00000637193.1:c.1871C>A
|
ENSP00000490734.1:p.Ala624Glu
|
|
ENST00000344462.8:c.2381C>A
|
ENSP00000339611.4:p.Ala794Glu
|
|
ENST00000357249.6:c.2042C>A
|
ENSP00000349789.3:p.Ala681Glu
|
|
ENST00000359125.6:c.2474C>A
|
ENSP00000352035.2:p.Ala825Glu
|
|
ENST00000360480.7:c.2390C>A
|
ENSP00000353668.3:p.Ala797Glu
|
|
ENST00000370224.5:c.2241+257C>A
|
ENSP00000359244.2:n.2241+257C>A
|
|
ENST00000625514.2:c.2205+257C>A
|
ENSP00000486040.1:n.2205+257C>A
|
|
ENST00000626839.2:c.2420C>A
|
ENSP00000486706.1:p.Ala807Glu
|
|
ENST00000629241.2:c.2133+257C>A
|
ENSP00000487142.1:n.2133+257C>A
|
|
ENST00000629676.2:c.1680-5946C>A
|
ENSP00000486194.1:n.1680-5946C>A
|
|
NM_004518.4:c.2390C>A
|
NP_004509.2:p.Ala797Glu
|
|
NM_172106.1:c.2420C>A
|
NP_742104.1:p.Ala807Glu
|
|
NM_172107.2:c.2474C>A
|
NP_742105.1:p.Ala825Glu
|
|
NM_172108.3:c.2381C>A
|
NP_742106.1:p.Ala794Glu
|
|
XM_006723787.1:c.2516C>A
|
XP_006723850.1:p.Ala839Glu
|
|
XM_011528807.1:c.2582C>A
|
XP_011527109.1:p.Ala861Glu
|
|
XM_011528808.1:c.2579C>A
|
XP_011527110.1:p.Ala860Glu
|
|
XM_011528809.1:c.2552C>A
|
XP_011527111.1:p.Ala851Glu
|
|
XM_011528810.1:c.2528C>A
|
XP_011527112.1:p.Ala843Glu
|
|
XM_011528811.1:c.2498C>A
|
XP_011527113.1:p.Ala833Glu
|
|
XM_011528812.1:c.2471C>A
|
XP_011527114.1:p.Ala824Glu
|
|
XM_011528813.1:c.2456C>A
|
XP_011527115.1:p.Ala819Glu
|
|
XM_011528814.1:c.2063C>A
|
XP_011527116.1:p.Ala688Glu
|
|
NM_004518.5:c.2390C>A
|
NP_004509.2:p.Ala797Glu
|
|
NM_172106.2:c.2420C>A
|
NP_742104.1:p.Ala807Glu
|
|
NM_172107.3:c.2474C>A
|
NP_742105.1:p.Ala825Glu
|
|
NM_172108.4:c.2381C>A
|
NP_742106.1:p.Ala794Glu
|
|
XM_011528810.2:c.2528C>A
|
XP_011527112.1:p.Ala843Glu
|
|
XM_011528811.2:c.2498C>A
|
XP_011527113.1:p.Ala833Glu
|
|
XM_017027841.2:c.2525C>A
|
XP_016883330.1:p.Ala842Glu
|
|
XM_017027842.2:c.2462C>A
|
XP_016883331.1:p.Ala821Glu
|
|
XM_017027843.1:c.2459C>A
|
XP_016883332.1:p.Ala820Glu
|
|
XM_017027844.2:c.2417C>A
|
XP_016883333.1:p.Ala806Glu
|
|
XM_017027845.1:c.1490C>A
|
XP_016883334.1:p.Ala497Glu
|
|
NM_004518.6:c.2390C>A
|
NP_004509.2:p.Ala797Glu
|
|
NM_172106.3:c.2420C>A
|
NP_742104.1:p.Ala807Glu
|
|
NM_172107.4:c.2474C>A
MANE Select
|
NP_742105.1:p.Ala825Glu
|
|
NM_172108.5:c.2381C>A
|
NP_742106.1:p.Ala794Glu
|
|
NM_001382235.1:c.2528C>A
|
NP_001369164.1:p.Ala843Glu
|
|