ENST00000504915.3:c.8032A>T
|
ENSP00000473355.2:p.Arg2678Ter
|
|
ENST00000505350.2:c.*7984A>T
|
ENSP00000481752.1:n.*7984A>T
|
|
ENST00000507379.6:c.7924A>T
|
ENSP00000423224.2:p.Arg2642Ter
|
|
ENST00000509732.6:c.7978A>T
|
ENSP00000426541.2:p.Arg2660Ter
|
|
ENST00000512211.7:c.7978A>T
|
ENSP00000423828.3:p.Arg2660Ter
|
|
ENST00000257430.9:c.7978A>T
MANE Select
|
ENSP00000257430.4:p.Arg2660Ter
|
|
ENST00000257430.8:c.7978A>T
|
ENSP00000257430.4:p.Arg2660Ter
|
|
ENST00000508376.6:c.7978A>T
|
ENSP00000427089.2:p.Arg2660Ter
|
|
ENST00000520401.1:c.231-13077A>T
|
|
|
NM_000038.5:c.7978A>T
|
NP_000029.2:p.Arg2660Ter
|
|
NM_001127510.2:c.7978A>T
|
NP_001120982.1:p.Arg2660Ter
|
|
NM_001127511.2:c.7924A>T
|
NP_001120983.2:p.Arg2642Ter
|
|
NM_001354895.1:c.7978A>T
|
NP_001341824.1:p.Arg2660Ter
|
|
NM_001354896.1:c.8032A>T
|
NP_001341825.1:p.Arg2678Ter
|
|
NM_001354897.1:c.8008A>T
|
NP_001341826.1:p.Arg2670Ter
|
|
NM_001354898.1:c.7903A>T
|
NP_001341827.1:p.Arg2635Ter
|
|
NM_001354899.1:c.7894A>T
|
NP_001341828.1:p.Arg2632Ter
|
|
NM_001354900.1:c.7855A>T
|
NP_001341829.1:p.Arg2619Ter
|
|
NM_001354901.1:c.7801A>T
|
NP_001341830.1:p.Arg2601Ter
|
|
NM_001354902.1:c.7705A>T
|
NP_001341831.1:p.Arg2569Ter
|
|
NM_001354903.1:c.7675A>T
|
NP_001341832.1:p.Arg2559Ter
|
|
NM_001354904.1:c.7600A>T
|
NP_001341833.1:p.Arg2534Ter
|
|
NM_001354905.1:c.7498A>T
|
NP_001341834.1:p.Arg2500Ter
|
|
NM_001354906.1:c.7129A>T
|
NP_001341835.1:p.Arg2377Ter
|
|
NM_000038.6:c.7978A>T
MANE Select
|
NP_000029.2:p.Arg2660Ter
|
|
NM_001127510.3:c.7978A>T
|
NP_001120982.1:p.Arg2660Ter
|
|
NM_001127511.3:c.7924A>T
|
NP_001120983.2:p.Arg2642Ter
|
|
NM_001354895.2:c.7978A>T
|
NP_001341824.1:p.Arg2660Ter
|
|
NM_001354896.2:c.8032A>T
|
NP_001341825.1:p.Arg2678Ter
|
|
NM_001354897.2:c.8008A>T
|
NP_001341826.1:p.Arg2670Ter
|
|
NM_001354898.2:c.7903A>T
|
NP_001341827.1:p.Arg2635Ter
|
|
NM_001354899.2:c.7894A>T
|
NP_001341828.1:p.Arg2632Ter
|
|
NM_001354900.2:c.7855A>T
|
NP_001341829.1:p.Arg2619Ter
|
|
NM_001354901.2:c.7801A>T
|
NP_001341830.1:p.Arg2601Ter
|
|
NM_001354902.2:c.7705A>T
|
NP_001341831.1:p.Arg2569Ter
|
|
NM_001354903.2:c.7675A>T
|
NP_001341832.1:p.Arg2559Ter
|
|
NM_001354904.2:c.7600A>T
|
NP_001341833.1:p.Arg2534Ter
|
|
NM_001354905.2:c.7498A>T
|
NP_001341834.1:p.Arg2500Ter
|
|
NM_001354906.2:c.7129A>T
|
NP_001341835.1:p.Arg2377Ter
|
|