ENST00000706989.1:c.2002A>G
|
ENSP00000516702.1:p.Ile668Val
|
|
ENST00000359125.7:c.1948A>G
MANE Select
|
ENSP00000352035.2:p.Ile650Val
|
|
ENST00000637193.1:c.1345A>G
|
ENSP00000490734.1:p.Ile449Val
|
|
ENST00000344462.8:c.1855A>G
|
ENSP00000339611.4:p.Ile619Val
|
|
ENST00000357249.6:c.1516A>G
|
ENSP00000349789.3:p.Ile506Val
|
|
ENST00000359125.6:c.1948A>G
|
ENSP00000352035.2:p.Ile650Val
|
|
ENST00000360480.7:c.1864A>G
|
ENSP00000353668.3:p.Ile622Val
|
|
ENST00000370224.5:c.1972A>G
|
ENSP00000359244.2:p.Ile658Val
|
|
ENST00000625514.2:c.1936A>G
|
ENSP00000486040.1:p.Ile646Val
|
|
ENST00000626839.2:c.1894A>G
|
ENSP00000486706.1:p.Ile632Val
|
|
ENST00000629241.2:c.1864A>G
|
ENSP00000487142.1:p.Ile622Val
|
|
ENST00000629676.2:c.1679+6135A>G
|
ENSP00000486194.1:n.1679+6135A>G
|
|
NM_004518.4:c.1864A>G
|
NP_004509.2:p.Ile622Val
|
|
NM_172106.1:c.1894A>G
|
NP_742104.1:p.Ile632Val
|
|
NM_172107.2:c.1948A>G
|
NP_742105.1:p.Ile650Val
|
|
NM_172108.3:c.1855A>G
|
NP_742106.1:p.Ile619Val
|
|
XM_006723787.1:c.1990A>G
|
XP_006723850.1:p.Ile664Val
|
|
XM_011528807.1:c.2056A>G
|
XP_011527109.1:p.Ile686Val
|
|
XM_011528808.1:c.2053A>G
|
XP_011527110.1:p.Ile685Val
|
|
XM_011528809.1:c.2026A>G
|
XP_011527111.1:p.Ile676Val
|
|
XM_011528810.1:c.2002A>G
|
XP_011527112.1:p.Ile668Val
|
|
XM_011528811.1:c.1972A>G
|
XP_011527113.1:p.Ile658Val
|
|
XM_011528812.1:c.1945A>G
|
XP_011527114.1:p.Ile649Val
|
|
XM_011528813.1:c.1930A>G
|
XP_011527115.1:p.Ile644Val
|
|
XM_011528814.1:c.1537A>G
|
XP_011527116.1:p.Ile513Val
|
|
NM_004518.5:c.1864A>G
|
NP_004509.2:p.Ile622Val
|
|
NM_172106.2:c.1894A>G
|
NP_742104.1:p.Ile632Val
|
|
NM_172107.3:c.1948A>G
|
NP_742105.1:p.Ile650Val
|
|
NM_172108.4:c.1855A>G
|
NP_742106.1:p.Ile619Val
|
|
XM_011528810.2:c.2002A>G
|
XP_011527112.1:p.Ile668Val
|
|
XM_011528811.2:c.1972A>G
|
XP_011527113.1:p.Ile658Val
|
|
XM_017027841.2:c.1999A>G
|
XP_016883330.1:p.Ile667Val
|
|
XM_017027842.2:c.1936A>G
|
XP_016883331.1:p.Ile646Val
|
|
XM_017027843.1:c.1933A>G
|
XP_016883332.1:p.Ile645Val
|
|
XM_017027844.2:c.1891A>G
|
XP_016883333.1:p.Ile631Val
|
|
XM_017027845.1:c.964A>G
|
XP_016883334.1:p.Ile322Val
|
|
NM_004518.6:c.1864A>G
|
NP_004509.2:p.Ile622Val
|
|
NM_172106.3:c.1894A>G
|
NP_742104.1:p.Ile632Val
|
|
NM_172107.4:c.1948A>G
MANE Select
|
NP_742105.1:p.Ile650Val
|
|
NM_172108.5:c.1855A>G
|
NP_742106.1:p.Ile619Val
|
|
NM_001382235.1:c.2002A>G
|
NP_001369164.1:p.Ile668Val
|
|