ENST00000388996.10:c.*5391C>T
MANE Select
|
ENSP00000373648.3:n.*5391C>T
|
|
ENST00000388996.8:c.*5391C>T
|
ENSP00000373648.3:n.*5391C>T
|
|
ENST00000621976.1:c.7647C>T
|
ENSP00000482510.1:n.7647C>T
|
|
NM_001204824.1:c.*5391C>T
|
NP_001191753.1:n.*5391C>T
|
|
NM_004519.3:c.*5391C>T
|
NP_004510.1:n.*5391C>T
|
|
XM_005250914.2:c.*5391C>T
|
XP_005250971.1:n.*5391C>T
|
|
XM_006716555.2:c.*5391C>T
|
XP_006716618.1:n.*5391C>T
|
|
XM_011517026.1:c.*5391C>T
|
XP_011515328.1:n.*5391C>T
|
|
XM_005250914.3:c.*5391C>T
|
XP_005250971.1:n.*5391C>T
|
|
XM_006716555.3:c.*5391C>T
|
XP_006716618.1:n.*5391C>T
|
|
XM_011517026.2:c.*5391C>T
|
XP_011515328.1:n.*5391C>T
|
|
XM_017013400.1:c.*5391C>T
|
XP_016868889.1:n.*5391C>T
|
|
NM_004519.4:c.*5391C>T
MANE Select
|
NP_004510.1:n.*5391C>T
|
|
NM_001204824.2:c.*5391C>T
|
NP_001191753.1:n.*5391C>T
|
|