ENST00000405460.9:c.16366A>T
MANE Select
|
ENSP00000384582.2:p.Lys5456Ter
|
|
ENST00000425867.3:c.5320A>T
|
ENSP00000392618.3:p.Lys1774Ter
|
|
ENST00000638510.1:n.3633A>T
|
|
|
ENST00000639431.1:c.265+147385A>T
|
ENSP00000491057.1:n.265+147385A>T
|
|
ENST00000640061.1:n.128+1412A>T
|
|
|
ENST00000640407.1:c.2776A>T
|
ENSP00000491425.1:p.Lys926Ter
|
|
ENST00000405460.6:c.16366A>T
|
ENSP00000384582.2:p.Lys5456Ter
|
|
ENST00000425867.2:c.3349A>T
|
ENSP00000392618.2:p.Lys1117Ter
|
|
NM_032119.3:c.16366A>T
|
NP_115495.3:p.Lys5456Ter
|
|
NR_003149.1:n.16379A>T
|
|
|
XM_011543675.1:c.16363A>T
|
XP_011541977.1:p.Lys5455Ter
|
|
XM_011543676.1:c.16285A>T
|
XP_011541978.1:p.Lys5429Ter
|
|
XM_011543677.1:c.13669A>T
|
XP_011541979.1:p.Lys4557Ter
|
|
NM_032119.4:c.16366A>T
MANE Select
|
NP_115495.3:p.Lys5456Ter
|
|
XM_017009963.2:c.16387A>T
|
XP_016865452.1:p.Lys5463Ter
|
|
XM_017009964.2:c.16384A>T
|
XP_016865453.1:p.Lys5462Ter
|
|
XM_017009965.1:c.16384A>T
|
XP_016865454.1:p.Lys5462Ter
|
|
XM_017009966.2:c.16306A>T
|
XP_016865455.1:p.Lys5436Ter
|
|
XM_017009967.1:c.16291A>T
|
XP_016865456.1:p.Lys5431Ter
|
|
XM_017009968.2:c.16207A>T
|
XP_016865457.1:p.Lys5403Ter
|
|
XM_017009969.2:c.16387A>T
|
XP_016865458.1:p.Lys5463Ter
|
|
XM_017009972.1:c.9505A>T
|
XP_016865461.1:p.Lys3169Ter
|
|
XM_017009973.1:c.9484A>T
|
XP_016865462.1:p.Lys3162Ter
|
|
NR_003149.2:n.16382A>T
|
|
|