ENST00000399503.4:c.2612T>A
MANE Select
|
ENSP00000382423.3:p.Leu871Ter
|
|
ENST00000399503.3:c.2612T>A
|
ENSP00000382423.3:p.Leu871Ter
|
|
NM_005921.1:c.2612T>A
|
NP_005912.1:p.Leu871Ter
|
|
XM_005248519.3:c.2234T>A
|
XP_005248576.2:p.Leu745Ter
|
|
XM_011543406.1:c.2357T>A
|
XP_011541708.1:p.Leu786Ter
|
|
XM_011543407.1:c.2333T>A
|
XP_011541709.1:p.Leu778Ter
|
|
XM_011543408.1:c.2612T>A
|
XP_011541710.1:p.Leu871Ter
|
|
XM_017009484.1:c.2201T>A
|
XP_016864973.1:p.Leu734Ter
|
|
XM_017009485.1:c.2123T>A
|
XP_016864974.1:p.Leu708Ter
|
|
XR_001742068.2:n.2643T>A
|
|
|
NM_005921.2:c.2612T>A
MANE Select
|
NP_005912.1:p.Leu871Ter
|
|