ENST00000399503.4:c.799C>A
MANE Select
|
ENSP00000382423.3:p.Pro267Thr
|
|
ENST00000399503.3:c.799C>A
|
ENSP00000382423.3:p.Pro267Thr
|
|
NM_005921.1:c.799C>A
|
NP_005912.1:p.Pro267Thr
|
|
XM_005248519.3:c.421C>A
|
XP_005248576.2:p.Pro141Thr
|
|
XM_011543406.1:c.544C>A
|
XP_011541708.1:p.Pro182Thr
|
|
XM_011543407.1:c.799C>A
|
XP_011541709.1:p.Pro267Thr
|
|
XM_011543408.1:c.799C>A
|
XP_011541710.1:p.Pro267Thr
|
|
XM_017009484.1:c.388C>A
|
XP_016864973.1:p.Pro130Thr
|
|
XM_017009485.1:c.310C>A
|
XP_016864974.1:p.Pro104Thr
|
|
XR_001742068.2:n.830C>A
|
|
|
NM_005921.2:c.799C>A
MANE Select
|
NP_005912.1:p.Pro267Thr
|
|