ENST00000294304.12:c.4600C>G
MANE Select
|
ENSP00000294304.6:p.Arg1534Gly
|
|
ENST00000294304.11:c.4600C>G
|
ENSP00000294304.6:p.Arg1534Gly
|
|
ENST00000529481.1:n.191C>G
|
|
|
ENST00000529702.1:c.270C>G
|
|
|
ENST00000529993.5:c.*3206C>G
|
ENSP00000436652.1:n.*3206C>G
|
|
NM_001291902.1:c.2857C>G
|
NP_001278831.1:p.Arg953Gly
|
|
NM_002335.3:c.4600C>G
|
NP_002326.2:p.Arg1534Gly
|
|
XM_005273994.2:c.4714C>G
|
XP_005274051.1:p.Arg1572Gly
|
|
XM_011545029.1:c.4741C>G
|
XP_011543331.1:p.Arg1581Gly
|
|
XM_011545030.1:c.4627C>G
|
XP_011543332.1:p.Arg1543Gly
|
|
XM_011545031.1:c.4757C>G
|
XP_011543333.1:p.Ser1586Trp
|
|
XR_949925.1:n.4987C>G
|
|
|
XR_949926.1:n.5003C>G
|
|
|
XM_017017735.1:c.2971C>G
|
XP_016873224.1:p.Arg991Gly
|
|
XM_017017736.1:c.2254C>G
|
XP_016873225.1:p.Arg752Gly
|
|
XR_949925.2:n.4987C>G
|
|
|
XR_949926.2:n.5003C>G
|
|
|
NM_002335.4:c.4600C>G
MANE Select
|
NP_002326.2:p.Arg1534Gly
|
|
NM_001291902.2:c.2857C>G
|
NP_001278831.1:p.Arg953Gly
|
|