ENST00000253270.13:c.752+1472A>G
MANE Select
|
ENSP00000253270.7:n.752+1472A>G
|
|
ENST00000375259.9:c.489-11076A>G
|
ENSP00000364408.4:n.489-11076A>G
|
|
ENST00000490599.2:c.444+1472A>G
|
|
|
ENST00000643789.1:c.354+1472A>G
|
|
|
ENST00000650065.1:c.717+1472A>G
|
|
|
ENST00000253270.11:c.752+1472A>G
|
ENSP00000253270.7:n.752+1472A>G
|
|
ENST00000375259.8:c.489-11076A>G
|
ENSP00000364408.4:n.489-11076A>G
|
|
NM_001286990.1:c.489-11076A>G
|
NP_001273919.1:n.489-11076A>G
|
|
NM_007001.2:c.752+1472A>G
|
NP_008932.2:n.752+1472A>G
|
|
NR_104627.1:n.828+1472A>G
|
|
|
XM_005251673.1:c.684+8659A>G
|
XP_005251730.1:n.684+8659A>G
|
|
XM_005251674.1:c.752+1472A>G
|
XP_005251731.1:n.752+1472A>G
|
|
XM_005251675.2:c.611+1472A>G
|
XP_005251732.1:n.611+1472A>G
|
|
XM_005251676.1:c.684+8659A>G
|
XP_005251733.1:n.684+8659A>G
|
|
XM_005251678.3:c.398+1472A>G
|
XP_005251735.1:n.398+1472A>G
|
|
XM_006716939.2:c.348-11076A>G
|
XP_006717002.1:n.348-11076A>G
|
|
XM_011518164.1:c.581+1472A>G
|
XP_011516466.1:n.581+1472A>G
|
|
XM_011518165.1:c.560+1472A>G
|
XP_011516467.1:n.560+1472A>G
|
|
XR_929705.1:n.735+8659A>G
|
|
|
XM_005251678.5:c.398+1472A>G
|
XP_005251735.1:n.398+1472A>G
|
|
XR_001746170.1:n.642+1472A>G
|
|
|
NM_007001.3:c.752+1472A>G
MANE Select
|
NP_008932.2:n.752+1472A>G
|
|
NM_001286990.2:c.489-11076A>G
|
NP_001273919.1:n.489-11076A>G
|
|
NR_104627.2:n.829+1472A>G
|
|
|