ENST00000704337.1:n.279C>G
|
|
|
ENST00000378536.5:c.1111C>G
MANE Select
|
ENSP00000367797.4:p.His371Asp
|
|
ENST00000378536.4:c.1111C>G
|
ENSP00000367797.4:p.His371Asp
|
|
ENST00000478223.2:n.218C>G
|
|
|
NM_003036.3:c.1111C>G
|
NP_003027.1:p.His371Asp
|
|
XM_005244775.2:c.1111C>G
|
XP_005244832.1:p.His371Asp
|
|
XM_005244776.3:c.241C>G
|
XP_005244833.1:p.His81Asp
|
|
XM_005244775.3:c.1111C>G
|
XP_005244832.1:p.His371Asp
|
|
XM_005244776.4:c.241C>G
|
XP_005244833.1:p.His81Asp
|
|
XM_017002128.1:c.619C>G
|
XP_016857617.1:p.His207Asp
|
|
NM_003036.4:c.1111C>G
MANE Select
|
NP_003027.1:p.His371Asp
|
|