ENST00000642418.1:n.1506G>C
|
|
|
ENST00000643693.1:n.970G>C
|
|
|
ENST00000644795.1:c.960G>C
|
ENSP00000495720.1:p.Gln320His
|
|
ENST00000646782.1:n.1902G>C
|
|
|
ENST00000647165.2:c.9168G>C
MANE Select
|
ENSP00000495481.1:p.Gln3056His
|
|
ENST00000651214.1:n.1673G>C
|
|
|
ENST00000205890.9:c.9168G>C
|
ENSP00000205890.5:p.Gln3056His
|
|
ENST00000418233.7:c.960G>C
|
ENSP00000408800.3:p.Gln320His
|
|
ENST00000433411.7:n.105G>C
|
|
|
ENST00000445289.6:n.316+1386G>C
|
|
|
ENST00000556535.5:c.30G>C
|
ENSP00000451782.1:p.Gln10His
|
|
ENST00000557190.5:n.70G>C
|
|
|
ENST00000557655.5:c.30G>C
|
ENSP00000451925.1:p.Gln10His
|
|
ENST00000578472.5:c.30G>C
|
ENSP00000467989.1:p.Gln10His
|
|
ENST00000615845.4:c.9168G>C
|
ENSP00000481642.1:p.Gln3056His
|
|
NM_016239.3:c.9168G>C
|
NP_057323.3:p.Gln3056His
|
|
XM_011523921.1:c.9162G>C
|
XP_011522223.1:p.Gln3054His
|
|
XM_017024714.2:c.9108G>C
|
XP_016880203.1:p.Gln3036His
|
|
XM_017024715.2:c.9171G>C
|
XP_016880204.1:p.Gln3057His
|
|
NM_016239.4:c.9168G>C
MANE Select
|
NP_057323.3:p.Gln3056His
|
|