ENST00000706989.1:c.2117A>C
|
ENSP00000516702.1:p.Lys706Thr
|
|
ENST00000359125.7:c.2063A>C
MANE Select
|
ENSP00000352035.2:p.Lys688Thr
|
|
ENST00000637193.1:c.1460A>C
|
ENSP00000490734.1:p.Lys487Thr
|
|
ENST00000344462.8:c.1970A>C
|
ENSP00000339611.4:p.Lys657Thr
|
|
ENST00000357249.6:c.1631A>C
|
ENSP00000349789.3:p.Lys544Thr
|
|
ENST00000359125.6:c.2063A>C
|
ENSP00000352035.2:p.Lys688Thr
|
|
ENST00000360480.7:c.1979A>C
|
ENSP00000353668.3:p.Lys660Thr
|
|
ENST00000370224.5:c.2087A>C
|
ENSP00000359244.2:p.Lys696Thr
|
|
ENST00000625514.2:c.2051A>C
|
ENSP00000486040.1:p.Lys684Thr
|
|
ENST00000626839.2:c.2009A>C
|
ENSP00000486706.1:p.Lys670Thr
|
|
ENST00000629241.2:c.1979A>C
|
ENSP00000487142.1:p.Lys660Thr
|
|
ENST00000629676.2:c.1679+6250A>C
|
ENSP00000486194.1:n.1679+6250A>C
|
|
NM_004518.4:c.1979A>C
|
NP_004509.2:p.Lys660Thr
|
|
NM_172106.1:c.2009A>C
|
NP_742104.1:p.Lys670Thr
|
|
NM_172107.2:c.2063A>C
|
NP_742105.1:p.Lys688Thr
|
|
NM_172108.3:c.1970A>C
|
NP_742106.1:p.Lys657Thr
|
|
XM_006723787.1:c.2105A>C
|
XP_006723850.1:p.Lys702Thr
|
|
XM_011528807.1:c.2171A>C
|
XP_011527109.1:p.Lys724Thr
|
|
XM_011528808.1:c.2168A>C
|
XP_011527110.1:p.Lys723Thr
|
|
XM_011528809.1:c.2141A>C
|
XP_011527111.1:p.Lys714Thr
|
|
XM_011528810.1:c.2117A>C
|
XP_011527112.1:p.Lys706Thr
|
|
XM_011528811.1:c.2087A>C
|
XP_011527113.1:p.Lys696Thr
|
|
XM_011528812.1:c.2060A>C
|
XP_011527114.1:p.Lys687Thr
|
|
XM_011528813.1:c.2045A>C
|
XP_011527115.1:p.Lys682Thr
|
|
XM_011528814.1:c.1652A>C
|
XP_011527116.1:p.Lys551Thr
|
|
NM_004518.5:c.1979A>C
|
NP_004509.2:p.Lys660Thr
|
|
NM_172106.2:c.2009A>C
|
NP_742104.1:p.Lys670Thr
|
|
NM_172107.3:c.2063A>C
|
NP_742105.1:p.Lys688Thr
|
|
NM_172108.4:c.1970A>C
|
NP_742106.1:p.Lys657Thr
|
|
XM_011528810.2:c.2117A>C
|
XP_011527112.1:p.Lys706Thr
|
|
XM_011528811.2:c.2087A>C
|
XP_011527113.1:p.Lys696Thr
|
|
XM_017027841.2:c.2114A>C
|
XP_016883330.1:p.Lys705Thr
|
|
XM_017027842.2:c.2051A>C
|
XP_016883331.1:p.Lys684Thr
|
|
XM_017027843.1:c.2048A>C
|
XP_016883332.1:p.Lys683Thr
|
|
XM_017027844.2:c.2006A>C
|
XP_016883333.1:p.Lys669Thr
|
|
XM_017027845.1:c.1079A>C
|
XP_016883334.1:p.Lys360Thr
|
|
NM_004518.6:c.1979A>C
|
NP_004509.2:p.Lys660Thr
|
|
NM_172106.3:c.2009A>C
|
NP_742104.1:p.Lys670Thr
|
|
NM_172107.4:c.2063A>C
MANE Select
|
NP_742105.1:p.Lys688Thr
|
|
NM_172108.5:c.1970A>C
|
NP_742106.1:p.Lys657Thr
|
|
NM_001382235.1:c.2117A>C
|
NP_001369164.1:p.Lys706Thr
|
|