ENST00000334785.12:c.*59T>C
MANE Select
|
ENSP00000333938.7:n.*59T>C
|
|
ENST00000330010.12:c.*59T>C
|
ENSP00000327363.8:n.*59T>C
|
|
ENST00000334785.11:c.*59T>C
|
ENSP00000333938.7:n.*59T>C
|
|
ENST00000342754.5:c.1717-12T>C
|
|
|
ENST00000480732.2:n.1661T>C
|
|
|
NM_001172309.1:c.*59T>C
|
NP_001165780.1:n.*59T>C
|
|
NM_144573.3:c.*59T>C , LRG_442t1:c.*59T>C
|
NP_653174.3:n.*59T>C
|
|
XM_005271322.2:c.2018-12T>C
|
XP_005271379.1:n.2018-12T>C
|
|
XM_005271323.2:c.1976-12T>C
|
XP_005271380.1:n.1976-12T>C
|
|
XM_005271324.3:c.1826-12T>C
|
XP_005271381.1:n.1826-12T>C
|
|
XM_005271325.2:c.1796-12T>C
|
XP_005271382.1:n.1796-12T>C
|
|
XM_005271326.2:c.1784-12T>C
|
XP_005271383.1:n.1784-12T>C
|
|
XM_005271327.2:c.1601-12T>C
|
XP_005271384.1:n.1601-12T>C
|
|
XM_005271322.4:c.2018-12T>C
|
XP_005271379.1:n.2018-12T>C
|
|
XM_005271323.4:c.1976-12T>C
|
XP_005271380.1:n.1976-12T>C
|
|
XM_005271324.5:c.1826-12T>C
|
XP_005271381.1:n.1826-12T>C
|
|
XM_005271325.4:c.1796-12T>C
|
XP_005271382.1:n.1796-12T>C
|
|
XM_005271326.4:c.1784-12T>C
|
XP_005271383.1:n.1784-12T>C
|
|
XM_005271327.4:c.1601-12T>C
|
XP_005271384.1:n.1601-12T>C
|
|
NM_001172309.2:c.*59T>C
|
NP_001165780.1:n.*59T>C
|
|
NM_144573.4:c.*59T>C
MANE Select
|
NP_653174.3:n.*59T>C
|
|