ENST00000378154.3:c.2355T>G
|
ENSP00000367396.2:p.Asn785Lys
|
|
ENST00000378158.6:c.2352T>G
|
ENSP00000367400.2:p.Asn784Lys
|
|
ENST00000378163.7:c.2406T>G
MANE Select
|
ENSP00000367405.1:p.Asn802Lys
|
|
ENST00000378166.9:c.2304T>G
|
ENSP00000367408.5:p.Asn768Lys
|
|
ENST00000378168.8:c.2409T>G
|
ENSP00000367410.4:p.Asn803Lys
|
|
ENST00000378179.9:c.1026T>G
|
ENSP00000367421.4:p.Asn342Lys
|
|
ENST00000421587.8:c.2337T>G
|
ENSP00000400526.4:p.Asn779Lys
|
|
ENST00000442742.7:c.2268T>G
|
ENSP00000398007.3:p.Asn756Lys
|
|
ENST00000642499.1:n.1185T>G
|
|
|
ENST00000643733.1:c.178T>G
|
|
|
ENST00000644219.1:c.2388T>G
|
ENSP00000495357.1:p.Asn796Lys
|
|
ENST00000644347.1:c.2319T>G
|
ENSP00000494183.1:p.Asn773Lys
|
|
ENST00000645566.1:c.2391T>G
|
ENSP00000494788.1:p.Asn797Lys
|
|
ENST00000645937.2:n.2637T>G
|
|
|
ENST00000645986.2:c.2373T>G
|
ENSP00000494409.2:p.Asn791Lys
|
|
ENST00000646087.2:c.1728T>G
|
ENSP00000495510.2:p.Asn576Lys
|
|
ENST00000646120.2:c.2322T>G
|
ENSP00000495291.2:p.Asn774Lys
|
|
ENST00000675354.1:c.2340T>G
|
ENSP00000502315.1:p.Asn780Lys
|
|
ENST00000378158.5:c.2355T>G
|
ENSP00000367400.1:p.Asn785Lys
|
|
ENST00000378163.5:c.2406T>G
|
ENSP00000367405.1:p.Asn802Lys
|
|
ENST00000378166.8:c.2391T>G
|
ENSP00000367408.4:p.Asn797Lys
|
|
ENST00000378168.6:c.771T>G
|
ENSP00000367410.2:p.Asn257Lys
|
|
ENST00000378179.7:c.1182T>G
|
ENSP00000367421.3:p.Asn394Lys
|
|
ENST00000421587.6:c.2319T>G
|
ENSP00000400526.2:p.Asn773Lys
|
|
ENST00000442742.6:c.2322T>G
|
ENSP00000398007.2:p.Asn774Lys
|
|
NM_001126054.2:c.2322T>G
|
NP_001119526.1:p.Asn774Lys
|
|
NM_001126055.2:c.2319T>G
|
NP_001119527.1:p.Asn773Lys
|
|
NM_003688.3:c.2391T>G
|
NP_003679.2:p.Asn797Lys
|
|
XM_005272686.3:c.2388T>G
|
XP_005272743.1:p.Asn796Lys
|
|
XM_006724566.2:c.2283T>G
|
XP_006724629.1:p.Asn761Lys
|
|
XM_011543993.1:c.2406T>G
|
XP_011542295.1:p.Asn802Lys
|
|
XM_011543994.1:c.2370T>G
|
XP_011542296.1:p.Asn790Lys
|
|
XM_011543995.1:c.2337T>G
|
XP_011542297.1:p.Asn779Lys
|
|
XM_011543996.1:c.2301T>G
|
XP_011542298.1:p.Asn767Lys
|
|
XM_011543997.1:c.1833T>G
|
XP_011542299.1:p.Asn611Lys
|
|
XM_005272686.4:c.2388T>G
|
XP_005272743.1:p.Asn796Lys
|
|
XM_006724566.3:c.2283T>G
|
XP_006724629.1:p.Asn761Lys
|
|
XM_011543993.2:c.2406T>G
|
XP_011542295.1:p.Asn802Lys
|
|
XM_011543994.2:c.2370T>G
|
XP_011542296.1:p.Asn790Lys
|
|
XM_011543995.2:c.2337T>G
|
XP_011542297.1:p.Asn779Lys
|
|
XM_011543996.2:c.2301T>G
|
XP_011542298.1:p.Asn767Lys
|
|
XM_011543997.3:c.1833T>G
|
XP_011542299.1:p.Asn611Lys
|
|
XM_024452473.1:c.1728T>G
|
XP_024308241.1:p.Asn576Lys
|
|
NM_001367721.1:c.2406T>G
MANE Select
|
NP_001354650.1:p.Asn802Lys
|
|