ENST00000525748.6:c.1396-176C>T
MANE Select
|
ENSP00000434364.2:n.1396-176C>T
|
|
ENST00000298923.11:c.*693-176C>T
|
ENSP00000298923.7:n.*693-176C>T
|
|
ENST00000525748.5:c.1396-176C>T
|
ENSP00000434364.1:n.1396-176C>T
|
|
NM_004211.3:c.1396-176C>T
|
NP_004202.2:n.1396-176C>T
|
|
XM_005253225.1:c.694-176C>T
|
XP_005253282.1:n.694-176C>T
|
|
XM_011520473.1:c.1396-176C>T
|
XP_011518775.1:n.1396-176C>T
|
|
NM_001318369.1:c.694-176C>T
|
NP_001305298.1:n.694-176C>T
|
|
NM_004211.4:c.1396-176C>T
|
NP_004202.3:n.1396-176C>T
|
|
XM_017018544.2:c.520-176C>T
|
XP_016874033.1:n.520-176C>T
|
|
XM_017018545.2:c.355-176C>T
|
XP_016874034.1:n.355-176C>T
|
|
NM_001318369.2:c.694-176C>T
|
NP_001305298.1:n.694-176C>T
|
|
NM_004211.5:c.1396-176C>T
MANE Select
|
NP_004202.4:n.1396-176C>T
|
|