ENST00000247933.9:c.1638G>T
|
ENSP00000247933.4:p.Lys546Asn
|
|
ENST00000514224.2:c.1638G>T
MANE Select
|
ENSP00000425081.2:p.Lys546Asn
|
|
ENST00000652070.1:n.1694G>T
|
|
|
ENST00000247933.8:c.1638G>T
|
ENSP00000247933.4:p.Lys546Asn
|
|
ENST00000514224.1:c.1242G>T
|
ENSP00000425081.1:p.Lys414Asn
|
|
ENST00000514417.1:n.30G>T
|
|
|
ENST00000514698.5:n.1745G>T
|
|
|
NM_000203.4:c.1638G>T
|
NP_000194.2:p.Lys546Asn
|
|
NR_110313.1:n.1726G>T
|
|
|
XM_006713882.2:c.1242G>T
|
XP_006713945.1:p.Lys414Asn
|
|
XM_011513459.1:c.1704G>T
|
XP_011511761.1:p.Lys568Asn
|
|
XM_011513460.1:c.1497G>T
|
XP_011511762.1:p.Lys499Asn
|
|
XM_011513461.1:c.1431G>T
|
XP_011511763.1:p.Lys477Asn
|
|
XM_011513462.1:c.1350G>T
|
XP_011511764.1:p.Lys450Asn
|
|
XM_011513463.1:c.1350G>T
|
XP_011511765.1:p.Lys450Asn
|
|
XR_924947.1:n.1894G>T
|
|
|
NM_000203.5:c.1638G>T
MANE Select
|
NP_000194.2:p.Lys546Asn
|
|
NM_001363576.1:c.1242G>T
|
NP_001350505.1:p.Lys414Asn
|
|
XM_011513461.2:c.1431G>T
|
XP_011511763.1:p.Lys477Asn
|
|
XM_017008163.1:c.678G>T
|
XP_016863652.1:p.Lys226Asn
|
|