ENST00000706989.1:c.1997T>C
|
ENSP00000516702.1:p.Met666Thr
|
|
ENST00000359125.7:c.1943T>C
MANE Select
|
ENSP00000352035.2:p.Met648Thr
|
|
ENST00000637193.1:c.1340T>C
|
ENSP00000490734.1:p.Met447Thr
|
|
ENST00000637338.1:n.100T>C
|
|
|
ENST00000344462.8:c.1850T>C
|
ENSP00000339611.4:p.Met617Thr
|
|
ENST00000357249.6:c.1511T>C
|
ENSP00000349789.3:p.Met504Thr
|
|
ENST00000359125.6:c.1943T>C
|
ENSP00000352035.2:p.Met648Thr
|
|
ENST00000360480.7:c.1859T>C
|
ENSP00000353668.3:p.Met620Thr
|
|
ENST00000370224.5:c.1967T>C
|
ENSP00000359244.2:p.Met656Thr
|
|
ENST00000625514.2:c.1931T>C
|
ENSP00000486040.1:p.Met644Thr
|
|
ENST00000626839.2:c.1889T>C
|
ENSP00000486706.1:p.Met630Thr
|
|
ENST00000629241.2:c.1859T>C
|
ENSP00000487142.1:p.Met620Thr
|
|
ENST00000629676.2:c.1679+6130T>C
|
ENSP00000486194.1:n.1679+6130T>C
|
|
NM_004518.4:c.1859T>C
|
NP_004509.2:p.Met620Thr
|
|
NM_172106.1:c.1889T>C
|
NP_742104.1:p.Met630Thr
|
|
NM_172107.2:c.1943T>C
|
NP_742105.1:p.Met648Thr
|
|
NM_172108.3:c.1850T>C
|
NP_742106.1:p.Met617Thr
|
|
XM_006723787.1:c.1985T>C
|
XP_006723850.1:p.Met662Thr
|
|
XM_011528807.1:c.2051T>C
|
XP_011527109.1:p.Met684Thr
|
|
XM_011528808.1:c.2048T>C
|
XP_011527110.1:p.Met683Thr
|
|
XM_011528809.1:c.2021T>C
|
XP_011527111.1:p.Met674Thr
|
|
XM_011528810.1:c.1997T>C
|
XP_011527112.1:p.Met666Thr
|
|
XM_011528811.1:c.1967T>C
|
XP_011527113.1:p.Met656Thr
|
|
XM_011528812.1:c.1940T>C
|
XP_011527114.1:p.Met647Thr
|
|
XM_011528813.1:c.1925T>C
|
XP_011527115.1:p.Met642Thr
|
|
XM_011528814.1:c.1532T>C
|
XP_011527116.1:p.Met511Thr
|
|
NM_004518.5:c.1859T>C
|
NP_004509.2:p.Met620Thr
|
|
NM_172106.2:c.1889T>C
|
NP_742104.1:p.Met630Thr
|
|
NM_172107.3:c.1943T>C
|
NP_742105.1:p.Met648Thr
|
|
NM_172108.4:c.1850T>C
|
NP_742106.1:p.Met617Thr
|
|
XM_011528810.2:c.1997T>C
|
XP_011527112.1:p.Met666Thr
|
|
XM_011528811.2:c.1967T>C
|
XP_011527113.1:p.Met656Thr
|
|
XM_017027841.2:c.1994T>C
|
XP_016883330.1:p.Met665Thr
|
|
XM_017027842.2:c.1931T>C
|
XP_016883331.1:p.Met644Thr
|
|
XM_017027843.1:c.1928T>C
|
XP_016883332.1:p.Met643Thr
|
|
XM_017027844.2:c.1886T>C
|
XP_016883333.1:p.Met629Thr
|
|
XM_017027845.1:c.959T>C
|
XP_016883334.1:p.Met320Thr
|
|
NM_004518.6:c.1859T>C
|
NP_004509.2:p.Met620Thr
|
|
NM_172106.3:c.1889T>C
|
NP_742104.1:p.Met630Thr
|
|
NM_172107.4:c.1943T>C
MANE Select
|
NP_742105.1:p.Met648Thr
|
|
NM_172108.5:c.1850T>C
|
NP_742106.1:p.Met617Thr
|
|
NM_001382235.1:c.1997T>C
|
NP_001369164.1:p.Met666Thr
|
|