ENST00000225573.5:c.584C>A
|
ENSP00000225573.5:p.Thr195Lys
|
|
ENST00000434554.7:c.659C>A
|
ENSP00000399960.3:p.Thr220Lys
|
|
ENST00000582171.6:c.*378C>A
|
ENSP00000463994.1:n.*378C>A
|
|
ENST00000583599.6:c.473C>A
|
ENSP00000463919.2:p.Thr158Lys
|
|
ENST00000584061.6:c.644C>A
|
ENSP00000463972.2:p.Thr215Lys
|
|
ENST00000584806.2:n.382C>A
|
|
|
ENST00000641305.1:n.2212C>A
|
|
|
ENST00000641323.1:c.*732C>A
|
ENSP00000492965.1:n.*732C>A
|
|
ENST00000641427.1:n.713C>A
|
|
|
ENST00000641511.1:c.445C>A
|
|
|
ENST00000641703.1:c.429C>A
|
ENSP00000493219.1:n.429C>A
|
|
ENST00000641709.1:c.*535C>A
|
ENSP00000493349.1:n.*535C>A
|
|
ENST00000641856.1:c.*1221C>A
|
ENSP00000493224.1:n.*1221C>A
|
|
ENST00000642017.2:c.713C>A
MANE Select
|
ENSP00000493302.2:p.Thr238Lys
|
|
ENST00000225573.4:c.713C>A
|
ENSP00000225573.4:p.Thr238Lys
|
|
ENST00000434554.6:c.584C>A
|
ENSP00000399960.2:p.Thr195Lys
|
|
ENST00000582171.5:c.*378C>A
|
ENSP00000463994.1:n.*378C>A
|
|
ENST00000584806.1:n.382C>A
|
|
|
ENST00000585320.5:c.*195C>A
|
ENSP00000462345.1:n.*195C>A
|
|
NM_018129.3:c.713C>A
|
NP_060599.1:p.Thr238Lys
|
|
XM_005257500.2:c.473C>A
|
XP_005257557.1:p.Thr158Lys
|
|
XM_011524968.1:c.428C>A
|
XP_011523270.1:p.Thr143Lys
|
|
XM_005257500.3:c.473C>A
|
XP_005257557.1:p.Thr158Lys
|
|
XM_011524968.2:c.428C>A
|
XP_011523270.1:p.Thr143Lys
|
|
XM_017024813.1:c.473C>A
|
XP_016880302.1:p.Thr158Lys
|
|
NM_018129.4:c.713C>A
MANE Select
|
NP_060599.1:p.Thr238Lys
|
|