ENST00000700061.1:c.1107C>G
|
|
|
ENST00000700062.1:c.1107C>G
|
|
|
ENST00000700065.1:n.3023C>G
|
|
|
ENST00000281513.10:c.3010C>G
MANE Select
|
ENSP00000281513.5:p.Arg1004Gly
|
|
ENST00000281513.9:c.3010C>G
|
ENSP00000281513.5:p.Arg1004Gly
|
|
ENST00000429842.1:c.302C>G
|
|
|
ENST00000441755.5:c.151C>G
|
ENSP00000396501.1:p.Arg51Gly
|
|
ENST00000442506.5:c.153C>G
|
|
|
NM_015909.3:c.3010C>G
|
NP_056993.2:p.Arg1004Gly
|
|
NR_052013.2:n.3054C>G
|
|
|
XM_011510357.1:c.2881C>G
|
XP_011508659.1:p.Arg961Gly
|
|
XM_011510358.1:c.3010C>G
|
XP_011508660.1:p.Arg1004Gly
|
|
XM_011510359.1:c.2371C>G
|
XP_011508661.1:p.Arg791Gly
|
|
XM_011510360.1:c.811C>G
|
XP_011508662.1:p.Arg271Gly
|
|
XM_011510361.1:c.802C>G
|
XP_011508663.1:p.Arg268Gly
|
|
XM_011510357.2:c.2881C>G
|
XP_011508659.1:p.Arg961Gly
|
|
XM_011510358.2:c.3010C>G
|
XP_011508660.1:p.Arg1004Gly
|
|
XM_011510360.2:c.811C>G
|
XP_011508662.1:p.Arg271Gly
|
|
XM_011510361.2:c.802C>G
|
XP_011508663.1:p.Arg268Gly
|
|
XM_017004317.1:c.3010C>G
|
XP_016859806.1:p.Arg1004Gly
|
|
XM_024452961.1:c.2371C>G
|
XP_024308729.1:p.Arg791Gly
|
|
NM_015909.4:c.3010C>G
MANE Select
|
NP_056993.2:p.Arg1004Gly
|
|
NR_052013.3:n.3040C>G
|
|
|