ENST00000649448.1:c.16G>A
|
ENSP00000497165.1:p.Val6Ile
|
|
ENST00000650372.1:c.1699G>A
MANE Select
|
ENSP00000497931.1:p.Val567Ile
|
|
ENST00000263817.6:c.1699G>A
|
ENSP00000263817.6:p.Val567Ile
|
|
ENST00000439188.1:c.388G>A
|
ENSP00000416058.1:n.388G>A
|
|
ENST00000478354.1:n.437G>A
|
|
|
NM_003742.2:c.1699G>A
|
NP_003733.2:p.Val567Ile
|
|
XM_006712817.2:c.1741G>A
|
XP_006712880.1:p.Val581Ile
|
|
XM_011512077.1:c.1801G>A
|
XP_011510379.1:p.Val601Ile
|
|
XM_011512078.1:c.1801G>A
|
XP_011510380.1:p.Val601Ile
|
|
XM_011512079.1:c.1801G>A
|
XP_011510381.1:p.Val601Ile
|
|
XM_011512080.1:c.1801G>A
|
XP_011510382.1:p.Val601Ile
|
|
XM_011512081.1:c.25G>A
|
XP_011510383.1:p.Val9Ile
|
|
NM_003742.4:c.1699G>A
MANE Select
|
NP_003733.2:p.Val567Ile
|
|
XM_006712817.3:c.1741G>A
|
XP_006712880.1:p.Val581Ile
|
|
XM_011512077.2:c.1801G>A
|
XP_011510379.1:p.Val601Ile
|
|
XM_011512078.2:c.1801G>A
|
XP_011510380.1:p.Val601Ile
|
|
XM_011512080.2:c.1801G>A
|
XP_011510382.1:p.Val601Ile
|
|
XM_011512081.2:c.25G>A
|
XP_011510383.1:p.Val9Ile
|
|
XM_017005165.1:c.1801G>A
|
XP_016860654.1:p.Val601Ile
|
|
XM_017005166.1:c.1030G>A
|
XP_016860655.1:p.Val344Ile
|
|
XM_017005167.1:c.484G>A
|
XP_016860656.1:p.Val162Ile
|
|