ENST00000547754.6:c.1167A>T
MANE Select
|
ENSP00000448955.1:p.Lys389Asn
|
|
ENST00000266754.9:c.1167A>T
|
ENSP00000266754.5:p.Lys389Asn
|
|
ENST00000537247.5:c.855A>T
|
ENSP00000442406.1:p.Lys285Asn
|
|
ENST00000539410.2:c.1167A>T
|
ENSP00000439672.1:p.Lys389Asn
|
|
ENST00000547754.5:c.1167A>T
|
ENSP00000448955.1:p.Lys389Asn
|
|
ENST00000552854.1:c.258A>T
|
ENSP00000450107.1:p.Lys86Asn
|
|
NM_001303130.1:c.1167A>T
|
NP_001290059.1:p.Lys389Asn
|
|
NM_001303131.1:c.855A>T
|
NP_001290060.1:p.Lys285Asn
|
|
NM_174942.2:c.1167A>T
|
NP_777602.1:p.Lys389Asn
|
|
XM_005268804.2:c.1167A>T
|
XP_005268861.1:p.Lys389Asn
|
|
XM_011538219.1:c.1167A>T
|
XP_011536521.1:p.Lys389Asn
|
|
XM_011538220.1:c.1167A>T
|
XP_011536522.1:p.Lys389Asn
|
|
XM_011538221.1:c.1167A>T
|
XP_011536523.1:p.Lys389Asn
|
|
XM_011538222.1:c.411A>T
|
XP_011536524.1:p.Lys137Asn
|
|
NM_001363672.1:c.1167A>T
|
NP_001350601.1:p.Lys389Asn
|
|
XM_005268804.3:c.1167A>T
|
XP_005268861.1:p.Lys389Asn
|
|
XM_011538220.2:c.1167A>T
|
XP_011536522.1:p.Lys389Asn
|
|
XM_011538221.2:c.1167A>T
|
XP_011536523.1:p.Lys389Asn
|
|
XM_017019206.1:c.1167A>T
|
XP_016874695.1:p.Lys389Asn
|
|
NM_174942.3:c.1167A>T
MANE Select
|
NP_777602.1:p.Lys389Asn
|
|
NM_001303130.2:c.1167A>T
|
NP_001290059.1:p.Lys389Asn
|
|
NM_001363672.2:c.1167A>T
|
NP_001350601.1:p.Lys389Asn
|
|
NM_001303131.2:c.855A>T
|
NP_001290060.1:p.Lys285Asn
|
|