ENST00000706989.1:c.2395C>A
|
ENSP00000516702.1:p.Leu799Met
|
|
ENST00000359125.7:c.2341C>A
MANE Select
|
ENSP00000352035.2:p.Leu781Met
|
|
ENST00000637193.1:c.1738C>A
|
ENSP00000490734.1:p.Leu580Met
|
|
ENST00000344462.8:c.2248C>A
|
ENSP00000339611.4:p.Leu750Met
|
|
ENST00000357249.6:c.1909C>A
|
ENSP00000349789.3:p.Leu637Met
|
|
ENST00000359125.6:c.2341C>A
|
ENSP00000352035.2:p.Leu781Met
|
|
ENST00000360480.7:c.2257C>A
|
ENSP00000353668.3:p.Leu753Met
|
|
ENST00000370224.5:c.2241+124C>A
|
ENSP00000359244.2:n.2241+124C>A
|
|
ENST00000625514.2:c.2205+124C>A
|
ENSP00000486040.1:n.2205+124C>A
|
|
ENST00000626839.2:c.2287C>A
|
ENSP00000486706.1:p.Leu763Met
|
|
ENST00000629241.2:c.2133+124C>A
|
ENSP00000487142.1:n.2133+124C>A
|
|
ENST00000629676.2:c.1680-6079C>A
|
ENSP00000486194.1:n.1680-6079C>A
|
|
NM_004518.4:c.2257C>A
|
NP_004509.2:p.Leu753Met
|
|
NM_172106.1:c.2287C>A
|
NP_742104.1:p.Leu763Met
|
|
NM_172107.2:c.2341C>A
|
NP_742105.1:p.Leu781Met
|
|
NM_172108.3:c.2248C>A
|
NP_742106.1:p.Leu750Met
|
|
XM_006723787.1:c.2383C>A
|
XP_006723850.1:p.Leu795Met
|
|
XM_011528807.1:c.2449C>A
|
XP_011527109.1:p.Leu817Met
|
|
XM_011528808.1:c.2446C>A
|
XP_011527110.1:p.Leu816Met
|
|
XM_011528809.1:c.2419C>A
|
XP_011527111.1:p.Leu807Met
|
|
XM_011528810.1:c.2395C>A
|
XP_011527112.1:p.Leu799Met
|
|
XM_011528811.1:c.2365C>A
|
XP_011527113.1:p.Leu789Met
|
|
XM_011528812.1:c.2338C>A
|
XP_011527114.1:p.Leu780Met
|
|
XM_011528813.1:c.2323C>A
|
XP_011527115.1:p.Leu775Met
|
|
XM_011528814.1:c.1930C>A
|
XP_011527116.1:p.Leu644Met
|
|
NM_004518.5:c.2257C>A
|
NP_004509.2:p.Leu753Met
|
|
NM_172106.2:c.2287C>A
|
NP_742104.1:p.Leu763Met
|
|
NM_172107.3:c.2341C>A
|
NP_742105.1:p.Leu781Met
|
|
NM_172108.4:c.2248C>A
|
NP_742106.1:p.Leu750Met
|
|
XM_011528810.2:c.2395C>A
|
XP_011527112.1:p.Leu799Met
|
|
XM_011528811.2:c.2365C>A
|
XP_011527113.1:p.Leu789Met
|
|
XM_017027841.2:c.2392C>A
|
XP_016883330.1:p.Leu798Met
|
|
XM_017027842.2:c.2329C>A
|
XP_016883331.1:p.Leu777Met
|
|
XM_017027843.1:c.2326C>A
|
XP_016883332.1:p.Leu776Met
|
|
XM_017027844.2:c.2284C>A
|
XP_016883333.1:p.Leu762Met
|
|
XM_017027845.1:c.1357C>A
|
XP_016883334.1:p.Leu453Met
|
|
NM_004518.6:c.2257C>A
|
NP_004509.2:p.Leu753Met
|
|
NM_172106.3:c.2287C>A
|
NP_742104.1:p.Leu763Met
|
|
NM_172107.4:c.2341C>A
MANE Select
|
NP_742105.1:p.Leu781Met
|
|
NM_172108.5:c.2248C>A
|
NP_742106.1:p.Leu750Met
|
|
NM_001382235.1:c.2395C>A
|
NP_001369164.1:p.Leu799Met
|
|