ENST00000357060.8:c.3408G>T
MANE Select
|
ENSP00000349568.3:p.Leu1136Phe
|
|
ENST00000357060.7:c.3408G>T
|
ENSP00000349568.3:p.Leu1136Phe
|
|
ENST00000434629.5:c.1490G>T
|
|
|
NM_025145.5:c.3408G>T
|
NP_079421.5:p.Leu1136Phe
|
|
XM_005270171.1:c.3411G>T
|
XP_005270228.1:p.Leu1137Phe
|
|
XM_005270172.2:c.3411G>T
|
XP_005270229.1:p.Leu1137Phe
|
|
XM_011540196.1:c.3525G>T
|
XP_011538498.1:p.Leu1175Phe
|
|
XM_011540197.1:c.3525G>T
|
XP_011538499.1:p.Leu1175Phe
|
|
XM_011540198.1:c.3408G>T
|
XP_011538500.1:p.Leu1136Phe
|
|
XM_011540199.1:c.3408G>T
|
XP_011538501.1:p.Leu1136Phe
|
|
XM_011540200.1:c.3525G>T
|
XP_011538502.1:p.Leu1175Phe
|
|
XM_011540201.1:c.3525G>T
|
XP_011538503.1:p.Leu1175Phe
|
|
XM_011540202.1:c.2754G>T
|
XP_011538504.1:p.Leu918Phe
|
|
XM_011540203.1:c.1308G>T
|
XP_011538505.1:p.Leu436Phe
|
|
NM_025145.6:c.3408G>T
|
NP_079421.5:p.Leu1136Phe
|
|
XM_005270171.2:c.3411G>T
|
XP_005270228.1:p.Leu1137Phe
|
|
XM_005270172.3:c.3411G>T
|
XP_005270229.1:p.Leu1137Phe
|
|
XM_011540196.2:c.3525G>T
|
XP_011538498.1:p.Leu1175Phe
|
|
XM_011540197.2:c.3525G>T
|
XP_011538499.1:p.Leu1175Phe
|
|
XM_011540198.2:c.3408G>T
|
XP_011538500.1:p.Leu1136Phe
|
|
XM_011540199.2:c.3408G>T
|
XP_011538501.1:p.Leu1136Phe
|
|
XM_011540200.2:c.3525G>T
|
XP_011538502.1:p.Leu1175Phe
|
|
XM_011540201.2:c.3525G>T
|
XP_011538503.1:p.Leu1175Phe
|
|
XM_011540202.2:c.2754G>T
|
XP_011538504.1:p.Leu918Phe
|
|
XM_017016681.1:c.3522G>T
|
XP_016872170.1:p.Leu1174Phe
|
|
XM_017016682.1:c.3177G>T
|
XP_016872171.1:p.Leu1059Phe
|
|
XM_024448177.1:c.1911G>T
|
XP_024303945.1:p.Leu637Phe
|
|
XM_024448178.1:c.1308G>T
|
XP_024303946.1:p.Leu436Phe
|
|
XR_002957015.1:n.3294G>T
|
|
|
NM_025145.7:c.3408G>T
MANE Select
|
NP_079421.5:p.Leu1136Phe
|
|