ENST00000323929.8:c.1784-103A>T
MANE Select
|
ENSP00000325863.4:n.1784-103A>T
|
|
ENST00000323929.7:c.1784-103A>T
|
ENSP00000325863.3:n.1784-103A>T
|
|
ENST00000323977.7:c.1783+1223A>T
|
ENSP00000326094.3:n.1783+1223A>T
|
|
ENST00000393241.8:c.1784-106A>T
|
ENSP00000376933.4:n.1784-106A>T
|
|
ENST00000407439.7:c.1793-103A>T
|
ENSP00000385614.3:n.1793-103A>T
|
|
ENST00000535120.1:n.83-106A>T
|
|
|
NM_005590.3:c.1783+1223A>T
|
NP_005581.2:n.1783+1223A>T
|
|
NM_005591.3:c.1784-103A>T , LRG_85t1:c.1784-103A>T
|
NP_005582.1:n.1784-103A>T
|
|
XM_005274008.2:c.1316-103A>T
|
XP_005274065.1:n.1316-103A>T
|
|
XM_006718842.2:c.1784-106A>T
|
XP_006718905.1:n.1784-106A>T
|
|
XM_011542837.1:c.1784-103A>T
|
XP_011541139.1:n.1784-103A>T
|
|
XR_947828.1:n.2080-103A>T
|
|
|
NM_001330347.1:c.1784-106A>T
|
NP_001317276.1:n.1784-106A>T
|
|
XM_005274008.3:c.1316-103A>T
|
XP_005274065.1:n.1316-103A>T
|
|
XM_006718842.3:c.1784-106A>T
|
XP_006718905.1:n.1784-106A>T
|
|
XM_011542837.2:c.1784-103A>T
|
XP_011541139.1:n.1784-103A>T
|
|
XM_017017772.1:c.1784-103A>T
|
XP_016873261.1:n.1784-103A>T
|
|
XR_947828.2:n.2080-103A>T
|
|
|
NM_001330347.2:c.1784-106A>T
|
NP_001317276.1:n.1784-106A>T
|
|
NM_005590.4:c.1783+1223A>T
|
NP_005581.2:n.1783+1223A>T
|
|
NM_005591.4:c.1784-103A>T
MANE Select
|
NP_005582.1:n.1784-103A>T
|
|