ENST00000706989.1:c.1970T>A
|
ENSP00000516702.1:p.Phe657Tyr
|
|
ENST00000359125.7:c.1916T>A
MANE Select
|
ENSP00000352035.2:p.Phe639Tyr
|
|
ENST00000637193.1:c.1313T>A
|
ENSP00000490734.1:p.Phe438Tyr
|
|
ENST00000637338.1:n.73T>A
|
|
|
ENST00000344462.8:c.1823T>A
|
ENSP00000339611.4:p.Phe608Tyr
|
|
ENST00000357249.6:c.1484T>A
|
ENSP00000349789.3:p.Phe495Tyr
|
|
ENST00000359125.6:c.1916T>A
|
ENSP00000352035.2:p.Phe639Tyr
|
|
ENST00000360480.7:c.1832T>A
|
ENSP00000353668.3:p.Phe611Tyr
|
|
ENST00000370224.5:c.1940T>A
|
ENSP00000359244.2:p.Phe647Tyr
|
|
ENST00000625514.2:c.1904T>A
|
ENSP00000486040.1:p.Phe635Tyr
|
|
ENST00000626839.2:c.1862T>A
|
ENSP00000486706.1:p.Phe621Tyr
|
|
ENST00000629241.2:c.1832T>A
|
ENSP00000487142.1:p.Phe611Tyr
|
|
ENST00000629676.2:c.1679+6103T>A
|
ENSP00000486194.1:n.1679+6103T>A
|
|
NM_004518.4:c.1832T>A
|
NP_004509.2:p.Phe611Tyr
|
|
NM_172106.1:c.1862T>A
|
NP_742104.1:p.Phe621Tyr
|
|
NM_172107.2:c.1916T>A
|
NP_742105.1:p.Phe639Tyr
|
|
NM_172108.3:c.1823T>A
|
NP_742106.1:p.Phe608Tyr
|
|
XM_006723787.1:c.1958T>A
|
XP_006723850.1:p.Phe653Tyr
|
|
XM_011528807.1:c.2024T>A
|
XP_011527109.1:p.Phe675Tyr
|
|
XM_011528808.1:c.2021T>A
|
XP_011527110.1:p.Phe674Tyr
|
|
XM_011528809.1:c.1994T>A
|
XP_011527111.1:p.Phe665Tyr
|
|
XM_011528810.1:c.1970T>A
|
XP_011527112.1:p.Phe657Tyr
|
|
XM_011528811.1:c.1940T>A
|
XP_011527113.1:p.Phe647Tyr
|
|
XM_011528812.1:c.1913T>A
|
XP_011527114.1:p.Phe638Tyr
|
|
XM_011528813.1:c.1898T>A
|
XP_011527115.1:p.Phe633Tyr
|
|
XM_011528814.1:c.1505T>A
|
XP_011527116.1:p.Phe502Tyr
|
|
NM_004518.5:c.1832T>A
|
NP_004509.2:p.Phe611Tyr
|
|
NM_172106.2:c.1862T>A
|
NP_742104.1:p.Phe621Tyr
|
|
NM_172107.3:c.1916T>A
|
NP_742105.1:p.Phe639Tyr
|
|
NM_172108.4:c.1823T>A
|
NP_742106.1:p.Phe608Tyr
|
|
XM_011528810.2:c.1970T>A
|
XP_011527112.1:p.Phe657Tyr
|
|
XM_011528811.2:c.1940T>A
|
XP_011527113.1:p.Phe647Tyr
|
|
XM_017027841.2:c.1967T>A
|
XP_016883330.1:p.Phe656Tyr
|
|
XM_017027842.2:c.1904T>A
|
XP_016883331.1:p.Phe635Tyr
|
|
XM_017027843.1:c.1901T>A
|
XP_016883332.1:p.Phe634Tyr
|
|
XM_017027844.2:c.1859T>A
|
XP_016883333.1:p.Phe620Tyr
|
|
XM_017027845.1:c.932T>A
|
XP_016883334.1:p.Phe311Tyr
|
|
NM_004518.6:c.1832T>A
|
NP_004509.2:p.Phe611Tyr
|
|
NM_172106.3:c.1862T>A
|
NP_742104.1:p.Phe621Tyr
|
|
NM_172107.4:c.1916T>A
MANE Select
|
NP_742105.1:p.Phe639Tyr
|
|
NM_172108.5:c.1823T>A
|
NP_742106.1:p.Phe608Tyr
|
|
NM_001382235.1:c.1970T>A
|
NP_001369164.1:p.Phe657Tyr
|
|