|
NM_021942.6:c.944A>G
MANE Select
|
NP_068761.4:p.His315Arg
|
|
ENST00000334690.11:c.944A>G
MANE Select
|
ENSP00000335371.6:p.His315Arg
|
|
NM_021942.5:c.944A>G
|
NP_068761.4:p.His315Arg
|
|
NM_199053.2:c.944A>G
|
NP_951008.1:p.His315Arg
|
|
NM_199053.3:c.944A>G
|
NP_951008.1:p.His315Arg
|
|
ENST00000334690.10:c.944A>G
|
ENSP00000335371.6:p.His315Arg
|
|
ENST00000357207.8:c.944A>G
|
ENSP00000349738.4:p.His315Arg
|
|
ENST00000505676.5:c.163-743A>G
|
ENSP00000422915.1:n.163-743A>G
|
|
XM_011532180.1:c.944A>G
|
XP_011530482.1:p.His315Arg
|
|
XM_017008537.2:c.944A>G
|
XP_016864026.1:p.His315Arg
|
|
XM_017008538.2:c.944A>G
|
XP_016864027.1:p.His315Arg
|
|
XM_024454179.1:c.944A>G
|
XP_024309947.1:p.His315Arg
|
|
XM_024454180.1:c.944A>G
|
XP_024309948.1:p.His315Arg
|
|
XM_024454181.1:c.-313A>G
|
XP_024309949.1:n.-313A>G
|
|
XR_001741315.2:n.1136A>G
|
|