ENST00000270301.12:c.4242C>G
|
ENSP00000270301.6:p.Asn1414Lys
|
|
ENST00000401500.7:c.4257C>G
MANE Select
|
ENSP00000384792.1:p.Asn1419Lys
|
|
ENST00000587391.6:c.*4117C>G
|
ENSP00000465525.1:n.*4117C>G
|
|
ENST00000679357.1:c.2337C>G
|
|
|
ENST00000679598.1:c.1002C>G
|
|
|
ENST00000679682.1:c.4242C>G
|
ENSP00000506226.1:p.Asn1414Lys
|
|
ENST00000679714.1:c.4251C>G
|
ENSP00000506627.1:p.Asn1417Lys
|
|
ENST00000679757.1:c.3906C>G
|
ENSP00000505158.1:p.Asn1302Lys
|
|
ENST00000679858.1:c.*3639C>G
|
ENSP00000505655.1:n.*3639C>G
|
|
ENST00000680211.1:c.858C>G
|
ENSP00000506102.1:p.Asn286Lys
|
|
ENST00000680280.1:n.1760C>G
|
|
|
ENST00000680349.1:n.2906C>G
|
|
|
ENST00000680403.1:c.4242C>G
|
ENSP00000505677.1:p.Asn1414Lys
|
|
ENST00000680564.1:c.4008C>G
|
ENSP00000505582.1:p.Asn1336Lys
|
|
ENST00000680590.1:c.*2637C>G
|
ENSP00000505350.1:n.*2637C>G
|
|
ENST00000680597.1:c.990C>G
|
|
|
ENST00000680739.1:c.1272C>G
|
|
|
ENST00000680773.1:n.2758C>G
|
|
|
ENST00000680806.1:c.*3560C>G
|
ENSP00000506418.1:n.*3560C>G
|
|
ENST00000680997.1:n.2189C>G
|
|
|
ENST00000681608.1:n.2102C>G
|
|
|
ENST00000681625.1:c.*1589C>G
|
ENSP00000505555.1:n.*1589C>G
|
|
ENST00000681648.1:n.2308C>G
|
|
|
ENST00000270301.11:c.4242C>G
|
ENSP00000270301.6:p.Asn1414Lys
|
|
ENST00000401500.6:c.4257C>G
|
ENSP00000384792.1:p.Asn1419Lys
|
|
ENST00000587391.5:c.*4117C>G
|
ENSP00000465525.1:n.*4117C>G
|
|
NM_001083961.1:c.4257C>G
|
NP_001077430.1:p.Asn1419Lys
|
|
NM_173636.4:c.4242C>G
|
NP_775907.4:p.Asn1414Lys
|
|
XM_005258809.2:c.4146C>G
|
XP_005258866.1:p.Asn1382Lys
|
|
XM_011526837.1:c.4242C>G
|
XP_011525139.1:p.Asn1414Lys
|
|
XM_011526838.1:c.4008C>G
|
XP_011525140.1:p.Asn1336Lys
|
|
XM_011526839.1:c.3906C>G
|
XP_011525141.1:p.Asn1302Lys
|
|
XM_011526840.1:c.3249C>G
|
XP_011525142.1:p.Asn1083Lys
|
|
XM_011526841.1:c.2835C>G
|
XP_011525143.1:p.Asn945Lys
|
|
XM_011526842.1:c.2688C>G
|
XP_011525144.1:p.Asn896Lys
|
|
XM_011526843.1:c.2004C>G
|
XP_011525145.1:p.Asn668Lys
|
|
XM_011526844.1:c.2004C>G
|
XP_011525146.1:p.Asn668Lys
|
|
XM_011526840.2:c.3249C>G
|
XP_011525142.1:p.Asn1083Lys
|
|
XM_011526841.2:c.2835C>G
|
XP_011525143.1:p.Asn945Lys
|
|
XM_011526844.2:c.2004C>G
|
XP_011525146.1:p.Asn668Lys
|
|
XM_017026665.1:c.4257C>G
|
XP_016882154.1:p.Asn1419Lys
|
|
NM_001083961.2:c.4257C>G
MANE Select
|
NP_001077430.1:p.Asn1419Lys
|
|
NM_173636.5:c.4242C>G
|
NP_775907.4:p.Asn1414Lys
|
|