ENST00000399503.4:c.3176G>A
MANE Select
|
ENSP00000382423.3:p.Arg1059Lys
|
|
ENST00000399503.3:c.3176G>A
|
ENSP00000382423.3:p.Arg1059Lys
|
|
NM_005921.1:c.3176G>A
|
NP_005912.1:p.Arg1059Lys
|
|
XM_005248519.3:c.2798G>A
|
XP_005248576.2:p.Arg933Lys
|
|
XM_011543406.1:c.2921G>A
|
XP_011541708.1:p.Arg974Lys
|
|
XM_011543407.1:c.2897G>A
|
XP_011541709.1:p.Arg966Lys
|
|
XM_011543408.1:c.3176G>A
|
XP_011541710.1:p.Arg1059Lys
|
|
XM_017009484.1:c.2765G>A
|
XP_016864973.1:p.Arg922Lys
|
|
XM_017009485.1:c.2687G>A
|
XP_016864974.1:p.Arg896Lys
|
|
XR_001742068.2:n.3207G>A
|
|
|
NM_005921.2:c.3176G>A
MANE Select
|
NP_005912.1:p.Arg1059Lys
|
|