ENST00000316386.11:c.501+354A>G
MANE Select
|
ENSP00000319476.6:n.501+354A>G
|
|
ENST00000316386.10:c.501+354A>G
|
ENSP00000319476.6:n.501+354A>G
|
|
ENST00000435193.1:c.501+354A>G
|
ENSP00000415951.1:n.501+354A>G
|
|
NM_012092.3:c.501+354A>G , LRG_65t1:c.501+354A>G
|
NP_036224.1:n.501+354A>G
|
|
XM_011511028.1:c.501+354A>G
|
XP_011509330.1:n.501+354A>G
|
|
XM_011511029.1:c.504+354A>G
|
XP_011509331.1:n.504+354A>G
|
|
XM_011511030.1:c.414+354A>G
|
XP_011509332.1:n.414+354A>G
|
|
XM_011511031.1:c.414+354A>G
|
XP_011509333.1:n.414+354A>G
|
|
NM_012092.4:c.501+354A>G
MANE Select
|
NP_036224.1:n.501+354A>G
|
|