ENST00000706989.1:c.2479C>A
|
ENSP00000516702.1:p.Gln827Lys
|
|
ENST00000359125.7:c.2425C>A
MANE Select
|
ENSP00000352035.2:p.Gln809Lys
|
|
ENST00000637193.1:c.1822C>A
|
ENSP00000490734.1:p.Gln608Lys
|
|
ENST00000344462.8:c.2332C>A
|
ENSP00000339611.4:p.Gln778Lys
|
|
ENST00000357249.6:c.1993C>A
|
ENSP00000349789.3:p.Gln665Lys
|
|
ENST00000359125.6:c.2425C>A
|
ENSP00000352035.2:p.Gln809Lys
|
|
ENST00000360480.7:c.2341C>A
|
ENSP00000353668.3:p.Gln781Lys
|
|
ENST00000370224.5:c.2241+208C>A
|
ENSP00000359244.2:n.2241+208C>A
|
|
ENST00000625514.2:c.2205+208C>A
|
ENSP00000486040.1:n.2205+208C>A
|
|
ENST00000626839.2:c.2371C>A
|
ENSP00000486706.1:p.Gln791Lys
|
|
ENST00000629241.2:c.2133+208C>A
|
ENSP00000487142.1:n.2133+208C>A
|
|
ENST00000629676.2:c.1680-5995C>A
|
ENSP00000486194.1:n.1680-5995C>A
|
|
NM_004518.4:c.2341C>A
|
NP_004509.2:p.Gln781Lys
|
|
NM_172106.1:c.2371C>A
|
NP_742104.1:p.Gln791Lys
|
|
NM_172107.2:c.2425C>A
|
NP_742105.1:p.Gln809Lys
|
|
NM_172108.3:c.2332C>A
|
NP_742106.1:p.Gln778Lys
|
|
XM_006723787.1:c.2467C>A
|
XP_006723850.1:p.Gln823Lys
|
|
XM_011528807.1:c.2533C>A
|
XP_011527109.1:p.Gln845Lys
|
|
XM_011528808.1:c.2530C>A
|
XP_011527110.1:p.Gln844Lys
|
|
XM_011528809.1:c.2503C>A
|
XP_011527111.1:p.Gln835Lys
|
|
XM_011528810.1:c.2479C>A
|
XP_011527112.1:p.Gln827Lys
|
|
XM_011528811.1:c.2449C>A
|
XP_011527113.1:p.Gln817Lys
|
|
XM_011528812.1:c.2422C>A
|
XP_011527114.1:p.Gln808Lys
|
|
XM_011528813.1:c.2407C>A
|
XP_011527115.1:p.Gln803Lys
|
|
XM_011528814.1:c.2014C>A
|
XP_011527116.1:p.Gln672Lys
|
|
NM_004518.5:c.2341C>A
|
NP_004509.2:p.Gln781Lys
|
|
NM_172106.2:c.2371C>A
|
NP_742104.1:p.Gln791Lys
|
|
NM_172107.3:c.2425C>A
|
NP_742105.1:p.Gln809Lys
|
|
NM_172108.4:c.2332C>A
|
NP_742106.1:p.Gln778Lys
|
|
XM_011528810.2:c.2479C>A
|
XP_011527112.1:p.Gln827Lys
|
|
XM_011528811.2:c.2449C>A
|
XP_011527113.1:p.Gln817Lys
|
|
XM_017027841.2:c.2476C>A
|
XP_016883330.1:p.Gln826Lys
|
|
XM_017027842.2:c.2413C>A
|
XP_016883331.1:p.Gln805Lys
|
|
XM_017027843.1:c.2410C>A
|
XP_016883332.1:p.Gln804Lys
|
|
XM_017027844.2:c.2368C>A
|
XP_016883333.1:p.Gln790Lys
|
|
XM_017027845.1:c.1441C>A
|
XP_016883334.1:p.Gln481Lys
|
|
NM_004518.6:c.2341C>A
|
NP_004509.2:p.Gln781Lys
|
|
NM_172106.3:c.2371C>A
|
NP_742104.1:p.Gln791Lys
|
|
NM_172107.4:c.2425C>A
MANE Select
|
NP_742105.1:p.Gln809Lys
|
|
NM_172108.5:c.2332C>A
|
NP_742106.1:p.Gln778Lys
|
|
NM_001382235.1:c.2479C>A
|
NP_001369164.1:p.Gln827Lys
|
|