ENST00000261693.11:c.*1700G>T
MANE Select
|
ENSP00000261693.6:n.*1700G>T
|
|
ENST00000339570.9:c.*1580G>T
|
ENSP00000343795.4:n.*1580G>T
|
|
NM_005505.5:c.*1700G>T
MANE Select
|
NP_005496.4:n.*1700G>T
|
|
NM_001082959.2:c.*1580G>T
|
NP_001076428.1:n.*1580G>T
|
|
NM_001367981.1:c.*1692G>T
|
NP_001354910.1:n.*1692G>T
|
|
NM_001367983.1:c.*1700G>T
|
NP_001354912.1:n.*1700G>T
|
|
NM_001367984.1:c.*1700G>T
|
NP_001354913.1:n.*1700G>T
|
|
NM_001367985.1:c.*1700G>T
|
NP_001354914.1:n.*1700G>T
|
|
NM_001367986.1:c.*1700G>T
|
NP_001354915.1:n.*1700G>T
|
|
NM_001367987.1:c.*1580G>T
|
NP_001354916.1:n.*1580G>T
|
|
NM_001367988.1:c.*1700G>T
|
NP_001354917.1:n.*1700G>T
|
|
NM_001367989.1:c.*1711G>T
|
NP_001354918.1:n.*1711G>T
|
|
NR_160416.1:n.3375G>T
|
|
|
NR_160417.1:n.3477G>T
|
|
|
NR_160418.1:n.2936G>T
|
|
|
NR_160419.1:n.3300G>T
|
|
|
NR_160420.1:n.3129G>T
|
|
|
NR_160421.1:n.3052G>T
|
|
|
NR_160422.1:n.3258G>T
|
|
|
NR_160423.1:n.3255G>T
|
|
|
NR_160424.1:n.3240G>T
|
|
|