ENST00000706989.1:c.2154C>G
|
ENSP00000516702.1:p.Asn718Lys
|
|
ENST00000359125.7:c.2100C>G
MANE Select
|
ENSP00000352035.2:p.Asn700Lys
|
|
ENST00000637193.1:c.1497C>G
|
ENSP00000490734.1:p.Asn499Lys
|
|
ENST00000344462.8:c.2007C>G
|
ENSP00000339611.4:p.Asn669Lys
|
|
ENST00000357249.6:c.1668C>G
|
ENSP00000349789.3:p.Asn556Lys
|
|
ENST00000359125.6:c.2100C>G
|
ENSP00000352035.2:p.Asn700Lys
|
|
ENST00000360480.7:c.2016C>G
|
ENSP00000353668.3:p.Asn672Lys
|
|
ENST00000370224.5:c.2124C>G
|
ENSP00000359244.2:p.Asn708Lys
|
|
ENST00000625514.2:c.2088C>G
|
ENSP00000486040.1:p.Asn696Lys
|
|
ENST00000626839.2:c.2046C>G
|
ENSP00000486706.1:p.Asn682Lys
|
|
ENST00000629241.2:c.2016C>G
|
ENSP00000487142.1:p.Asn672Lys
|
|
ENST00000629676.2:c.1679+6287C>G
|
ENSP00000486194.1:n.1679+6287C>G
|
|
NM_004518.4:c.2016C>G
|
NP_004509.2:p.Asn672Lys
|
|
NM_172106.1:c.2046C>G
|
NP_742104.1:p.Asn682Lys
|
|
NM_172107.2:c.2100C>G
|
NP_742105.1:p.Asn700Lys
|
|
NM_172108.3:c.2007C>G
|
NP_742106.1:p.Asn669Lys
|
|
XM_006723787.1:c.2142C>G
|
XP_006723850.1:p.Asn714Lys
|
|
XM_011528807.1:c.2208C>G
|
XP_011527109.1:p.Asn736Lys
|
|
XM_011528808.1:c.2205C>G
|
XP_011527110.1:p.Asn735Lys
|
|
XM_011528809.1:c.2178C>G
|
XP_011527111.1:p.Asn726Lys
|
|
XM_011528810.1:c.2154C>G
|
XP_011527112.1:p.Asn718Lys
|
|
XM_011528811.1:c.2124C>G
|
XP_011527113.1:p.Asn708Lys
|
|
XM_011528812.1:c.2097C>G
|
XP_011527114.1:p.Asn699Lys
|
|
XM_011528813.1:c.2082C>G
|
XP_011527115.1:p.Asn694Lys
|
|
XM_011528814.1:c.1689C>G
|
XP_011527116.1:p.Asn563Lys
|
|
NM_004518.5:c.2016C>G
|
NP_004509.2:p.Asn672Lys
|
|
NM_172106.2:c.2046C>G
|
NP_742104.1:p.Asn682Lys
|
|
NM_172107.3:c.2100C>G
|
NP_742105.1:p.Asn700Lys
|
|
NM_172108.4:c.2007C>G
|
NP_742106.1:p.Asn669Lys
|
|
XM_011528810.2:c.2154C>G
|
XP_011527112.1:p.Asn718Lys
|
|
XM_011528811.2:c.2124C>G
|
XP_011527113.1:p.Asn708Lys
|
|
XM_017027841.2:c.2151C>G
|
XP_016883330.1:p.Asn717Lys
|
|
XM_017027842.2:c.2088C>G
|
XP_016883331.1:p.Asn696Lys
|
|
XM_017027843.1:c.2085C>G
|
XP_016883332.1:p.Asn695Lys
|
|
XM_017027844.2:c.2043C>G
|
XP_016883333.1:p.Asn681Lys
|
|
XM_017027845.1:c.1116C>G
|
XP_016883334.1:p.Asn372Lys
|
|
NM_004518.6:c.2016C>G
|
NP_004509.2:p.Asn672Lys
|
|
NM_172106.3:c.2046C>G
|
NP_742104.1:p.Asn682Lys
|
|
NM_172107.4:c.2100C>G
MANE Select
|
NP_742105.1:p.Asn700Lys
|
|
NM_172108.5:c.2007C>G
|
NP_742106.1:p.Asn669Lys
|
|
NM_001382235.1:c.2154C>G
|
NP_001369164.1:p.Asn718Lys
|
|