ENST00000261693.11:c.1128G>T
MANE Select
|
ENSP00000261693.6:p.Pro376=
|
|
ENST00000679605.1:c.*128+7637G>T
|
ENSP00000505370.1:n.*128+7637G>T
|
|
ENST00000679955.1:n.2852G>T
|
|
|
ENST00000680556.1:c.1004+7642G>T
|
ENSP00000505757.1:n.1004+7642G>T
|
|
ENST00000680596.1:c.1104G>T
|
ENSP00000505605.1:p.Pro368=
|
|
ENST00000680926.1:c.*76G>T
|
ENSP00000505571.1:n.*76G>T
|
|
ENST00000680982.1:c.*1111G>T
|
ENSP00000506281.1:n.*1111G>T
|
|
ENST00000681117.1:c.*247G>T
|
ENSP00000506693.1:n.*247G>T
|
|
ENST00000681499.1:n.1001G>T
|
|
|
ENST00000681555.1:n.818G>T
|
|
|
ENST00000681686.1:c.1128G>T
|
ENSP00000505406.1:p.Pro376=
|
|
ENST00000261693.10:c.1128G>T
|
ENSP00000261693.6:p.Pro376=
|
|
ENST00000339570.9:c.1128G>T
|
ENSP00000343795.4:p.Pro376=
|
|
ENST00000415380.6:c.1128G>T
|
ENSP00000414979.2:p.Pro376=
|
|
ENST00000535005.5:n.1443G>T
|
|
|
ENST00000538291.5:n.1271G>T
|
|
|
ENST00000544327.1:c.966G>T
|
ENSP00000444851.1:p.Pro322=
|
|
ENST00000546215.5:c.1128G>T
|
ENSP00000442862.1:p.Pro376=
|
|
NM_001082959.1:c.1128G>T
|
NP_001076428.1:p.Pro376=
|
|
NM_005505.4:c.1128G>T
|
NP_005496.4:p.Pro376=
|
|
NM_005505.5:c.1128G>T
MANE Select
|
NP_005496.4:p.Pro376=
|
|
NM_001082959.2:c.1128G>T
|
NP_001076428.1:p.Pro376=
|
|
NM_001367981.1:c.1128G>T
|
NP_001354910.1:p.Pro376=
|
|
NM_001367982.1:c.1005G>T
|
NP_001354911.1:p.Pro335=
|
|
NM_001367983.1:c.1128G>T
|
NP_001354912.1:p.Pro376=
|
|
NM_001367984.1:c.1128G>T
|
NP_001354913.1:p.Pro376=
|
|
NM_001367985.1:c.1104G>T
|
NP_001354914.1:p.Pro368=
|
|
NM_001367986.1:c.1128G>T
|
NP_001354915.1:p.Pro376=
|
|
NM_001367987.1:c.1004+7642G>T
|
NP_001354916.1:n.1004+7642G>T
|
|
NM_001367988.1:c.727-4856G>T
|
NP_001354917.1:n.727-4856G>T
|
|
NM_001367989.1:c.1128G>T
|
NP_001354918.1:p.Pro376=
|
|
NR_160416.1:n.1272G>T
|
|
|
NR_160417.1:n.1272G>T
|
|
|
NR_160418.1:n.1037+7637G>T
|
|
|
NR_160419.1:n.1272G>T
|
|
|
NR_160420.1:n.1156G>T
|
|
|
NR_160421.1:n.1153+7637G>T
|
|
|
NR_160422.1:n.1156G>T
|
|
|
NR_160423.1:n.1154-4856G>T
|
|
|
NR_160424.1:n.1267G>T
|
|
|