ENST00000270301.12:c.4245C>G
|
ENSP00000270301.6:p.Ile1415Met
|
|
ENST00000401500.7:c.4260C>G
MANE Select
|
ENSP00000384792.1:p.Ile1420Met
|
|
ENST00000587391.6:c.*4120C>G
|
ENSP00000465525.1:n.*4120C>G
|
|
ENST00000679357.1:c.2340C>G
|
|
|
ENST00000679598.1:c.1005C>G
|
|
|
ENST00000679682.1:c.4245C>G
|
ENSP00000506226.1:p.Ile1415Met
|
|
ENST00000679714.1:c.4254C>G
|
ENSP00000506627.1:p.Ile1418Met
|
|
ENST00000679757.1:c.3909C>G
|
ENSP00000505158.1:p.Ile1303Met
|
|
ENST00000679858.1:c.*3642C>G
|
ENSP00000505655.1:n.*3642C>G
|
|
ENST00000680211.1:c.861C>G
|
ENSP00000506102.1:p.Ile287Met
|
|
ENST00000680280.1:n.1763C>G
|
|
|
ENST00000680349.1:n.2909C>G
|
|
|
ENST00000680403.1:c.4245C>G
|
ENSP00000505677.1:p.Ile1415Met
|
|
ENST00000680564.1:c.4011C>G
|
ENSP00000505582.1:p.Ile1337Met
|
|
ENST00000680590.1:c.*2640C>G
|
ENSP00000505350.1:n.*2640C>G
|
|
ENST00000680597.1:c.993C>G
|
|
|
ENST00000680739.1:c.1275C>G
|
|
|
ENST00000680773.1:n.2761C>G
|
|
|
ENST00000680806.1:c.*3563C>G
|
ENSP00000506418.1:n.*3563C>G
|
|
ENST00000680997.1:n.2192C>G
|
|
|
ENST00000681608.1:n.2105C>G
|
|
|
ENST00000681625.1:c.*1592C>G
|
ENSP00000505555.1:n.*1592C>G
|
|
ENST00000681648.1:n.2311C>G
|
|
|
ENST00000270301.11:c.4245C>G
|
ENSP00000270301.6:p.Ile1415Met
|
|
ENST00000401500.6:c.4260C>G
|
ENSP00000384792.1:p.Ile1420Met
|
|
ENST00000587391.5:c.*4120C>G
|
ENSP00000465525.1:n.*4120C>G
|
|
NM_001083961.1:c.4260C>G
|
NP_001077430.1:p.Ile1420Met
|
|
NM_173636.4:c.4245C>G
|
NP_775907.4:p.Ile1415Met
|
|
XM_005258809.2:c.4149C>G
|
XP_005258866.1:p.Ile1383Met
|
|
XM_011526837.1:c.4245C>G
|
XP_011525139.1:p.Ile1415Met
|
|
XM_011526838.1:c.4011C>G
|
XP_011525140.1:p.Ile1337Met
|
|
XM_011526839.1:c.3909C>G
|
XP_011525141.1:p.Ile1303Met
|
|
XM_011526840.1:c.3252C>G
|
XP_011525142.1:p.Ile1084Met
|
|
XM_011526841.1:c.2838C>G
|
XP_011525143.1:p.Ile946Met
|
|
XM_011526842.1:c.2691C>G
|
XP_011525144.1:p.Ile897Met
|
|
XM_011526843.1:c.2007C>G
|
XP_011525145.1:p.Ile669Met
|
|
XM_011526844.1:c.2007C>G
|
XP_011525146.1:p.Ile669Met
|
|
XM_011526840.2:c.3252C>G
|
XP_011525142.1:p.Ile1084Met
|
|
XM_011526841.2:c.2838C>G
|
XP_011525143.1:p.Ile946Met
|
|
XM_011526844.2:c.2007C>G
|
XP_011525146.1:p.Ile669Met
|
|
XM_017026665.1:c.4260C>G
|
XP_016882154.1:p.Ile1420Met
|
|
NM_001083961.2:c.4260C>G
MANE Select
|
NP_001077430.1:p.Ile1420Met
|
|
NM_173636.5:c.4245C>G
|
NP_775907.4:p.Ile1415Met
|
|