ENST00000706989.1:c.1496T>C
|
ENSP00000516702.1:p.Ile499Thr
|
|
ENST00000359125.7:c.1550T>C
MANE Select
|
ENSP00000352035.2:p.Ile517Thr
|
|
ENST00000637193.1:c.947T>C
|
ENSP00000490734.1:p.Ile316Thr
|
|
ENST00000344462.8:c.1457T>C
|
ENSP00000339611.4:p.Ile486Thr
|
|
ENST00000357249.6:c.1118T>C
|
ENSP00000349789.3:p.Ile373Thr
|
|
ENST00000359125.6:c.1550T>C
|
ENSP00000352035.2:p.Ile517Thr
|
|
ENST00000360480.7:c.1466T>C
|
ENSP00000353668.3:p.Ile489Thr
|
|
ENST00000370224.5:c.1466T>C
|
ENSP00000359244.2:p.Ile489Thr
|
|
ENST00000625514.2:c.1430T>C
|
ENSP00000486040.1:p.Ile477Thr
|
|
ENST00000626839.2:c.1496T>C
|
ENSP00000486706.1:p.Ile499Thr
|
|
ENST00000627221.2:c.607T>C
|
|
|
ENST00000629241.2:c.1466T>C
|
ENSP00000487142.1:p.Ile489Thr
|
|
ENST00000629318.1:c.158T>C
|
ENSP00000487384.1:p.Ile53Thr
|
|
ENST00000629676.2:c.1466T>C
|
ENSP00000486194.1:p.Ile489Thr
|
|
NM_004518.4:c.1466T>C
|
NP_004509.2:p.Ile489Thr
|
|
NM_172106.1:c.1496T>C
|
NP_742104.1:p.Ile499Thr
|
|
NM_172107.2:c.1550T>C
|
NP_742105.1:p.Ile517Thr
|
|
NM_172108.3:c.1457T>C
|
NP_742106.1:p.Ile486Thr
|
|
XM_006723787.1:c.1550T>C
|
XP_006723850.1:p.Ile517Thr
|
|
XM_011528807.1:c.1550T>C
|
XP_011527109.1:p.Ile517Thr
|
|
XM_011528808.1:c.1547T>C
|
XP_011527110.1:p.Ile516Thr
|
|
XM_011528809.1:c.1520T>C
|
XP_011527111.1:p.Ile507Thr
|
|
XM_011528810.1:c.1496T>C
|
XP_011527112.1:p.Ile499Thr
|
|
XM_011528811.1:c.1466T>C
|
XP_011527113.1:p.Ile489Thr
|
|
XM_011528812.1:c.1547T>C
|
XP_011527114.1:p.Ile516Thr
|
|
XM_011528813.1:c.1424T>C
|
XP_011527115.1:p.Ile475Thr
|
|
XM_011528814.1:c.1031T>C
|
XP_011527116.1:p.Ile344Thr
|
|
XM_011528815.1:c.1550T>C
|
XP_011527117.1:p.Ile517Thr
|
|
NM_004518.5:c.1466T>C
|
NP_004509.2:p.Ile489Thr
|
|
NM_172106.2:c.1496T>C
|
NP_742104.1:p.Ile499Thr
|
|
NM_172107.3:c.1550T>C
|
NP_742105.1:p.Ile517Thr
|
|
NM_172108.4:c.1457T>C
|
NP_742106.1:p.Ile486Thr
|
|
XM_011528810.2:c.1496T>C
|
XP_011527112.1:p.Ile499Thr
|
|
XM_011528811.2:c.1466T>C
|
XP_011527113.1:p.Ile489Thr
|
|
XM_017027841.2:c.1493T>C
|
XP_016883330.1:p.Ile498Thr
|
|
XM_017027842.2:c.1496T>C
|
XP_016883331.1:p.Ile499Thr
|
|
XM_017027843.1:c.1427T>C
|
XP_016883332.1:p.Ile476Thr
|
|
XM_017027844.2:c.1493T>C
|
XP_016883333.1:p.Ile498Thr
|
|
XM_017027845.1:c.458T>C
|
XP_016883334.1:p.Ile153Thr
|
|
NM_004518.6:c.1466T>C
|
NP_004509.2:p.Ile489Thr
|
|
NM_172106.3:c.1496T>C
|
NP_742104.1:p.Ile499Thr
|
|
NM_172107.4:c.1550T>C
MANE Select
|
NP_742105.1:p.Ile517Thr
|
|
NM_172108.5:c.1457T>C
|
NP_742106.1:p.Ile486Thr
|
|
NM_001382235.1:c.1496T>C
|
NP_001369164.1:p.Ile499Thr
|
|