ENST00000706989.1:c.2010G>T
|
ENSP00000516702.1:p.Pro670=
|
|
ENST00000359125.7:c.1956G>T
MANE Select
|
ENSP00000352035.2:p.Pro652=
|
|
ENST00000637193.1:c.1353G>T
|
ENSP00000490734.1:p.Pro451=
|
|
ENST00000344462.8:c.1863G>T
|
ENSP00000339611.4:p.Pro621=
|
|
ENST00000357249.6:c.1524G>T
|
ENSP00000349789.3:p.Pro508=
|
|
ENST00000359125.6:c.1956G>T
|
ENSP00000352035.2:p.Pro652=
|
|
ENST00000360480.7:c.1872G>T
|
ENSP00000353668.3:p.Pro624=
|
|
ENST00000370224.5:c.1980G>T
|
ENSP00000359244.2:p.Pro660=
|
|
ENST00000625514.2:c.1944G>T
|
ENSP00000486040.1:p.Pro648=
|
|
ENST00000626839.2:c.1902G>T
|
ENSP00000486706.1:p.Pro634=
|
|
ENST00000629241.2:c.1872G>T
|
ENSP00000487142.1:p.Pro624=
|
|
ENST00000629676.2:c.1679+6143G>T
|
ENSP00000486194.1:n.1679+6143G>T
|
|
NM_004518.4:c.1872G>T
|
NP_004509.2:p.Pro624=
|
|
NM_172106.1:c.1902G>T
|
NP_742104.1:p.Pro634=
|
|
NM_172107.2:c.1956G>T
|
NP_742105.1:p.Pro652=
|
|
NM_172108.3:c.1863G>T
|
NP_742106.1:p.Pro621=
|
|
XM_006723787.1:c.1998G>T
|
XP_006723850.1:p.Pro666=
|
|
XM_011528807.1:c.2064G>T
|
XP_011527109.1:p.Pro688=
|
|
XM_011528808.1:c.2061G>T
|
XP_011527110.1:p.Pro687=
|
|
XM_011528809.1:c.2034G>T
|
XP_011527111.1:p.Pro678=
|
|
XM_011528810.1:c.2010G>T
|
XP_011527112.1:p.Pro670=
|
|
XM_011528811.1:c.1980G>T
|
XP_011527113.1:p.Pro660=
|
|
XM_011528812.1:c.1953G>T
|
XP_011527114.1:p.Pro651=
|
|
XM_011528813.1:c.1938G>T
|
XP_011527115.1:p.Pro646=
|
|
XM_011528814.1:c.1545G>T
|
XP_011527116.1:p.Pro515=
|
|
NM_004518.5:c.1872G>T
|
NP_004509.2:p.Pro624=
|
|
NM_172106.2:c.1902G>T
|
NP_742104.1:p.Pro634=
|
|
NM_172107.3:c.1956G>T
|
NP_742105.1:p.Pro652=
|
|
NM_172108.4:c.1863G>T
|
NP_742106.1:p.Pro621=
|
|
XM_011528810.2:c.2010G>T
|
XP_011527112.1:p.Pro670=
|
|
XM_011528811.2:c.1980G>T
|
XP_011527113.1:p.Pro660=
|
|
XM_017027841.2:c.2007G>T
|
XP_016883330.1:p.Pro669=
|
|
XM_017027842.2:c.1944G>T
|
XP_016883331.1:p.Pro648=
|
|
XM_017027843.1:c.1941G>T
|
XP_016883332.1:p.Pro647=
|
|
XM_017027844.2:c.1899G>T
|
XP_016883333.1:p.Pro633=
|
|
XM_017027845.1:c.972G>T
|
XP_016883334.1:p.Pro324=
|
|
NM_004518.6:c.1872G>T
|
NP_004509.2:p.Pro624=
|
|
NM_172106.3:c.1902G>T
|
NP_742104.1:p.Pro634=
|
|
NM_172107.4:c.1956G>T
MANE Select
|
NP_742105.1:p.Pro652=
|
|
NM_172108.5:c.1863G>T
|
NP_742106.1:p.Pro621=
|
|
NM_001382235.1:c.2010G>T
|
NP_001369164.1:p.Pro670=
|
|