ENST00000682422.1:n.705-26G>T
|
|
|
ENST00000682545.1:c.*104G>T
|
ENSP00000508402.1:n.*104G>T
|
|
ENST00000682887.1:c.1499G>T
|
ENSP00000506946.1:n.1499G>T
|
|
ENST00000683302.1:c.1029G>T
|
ENSP00000507885.1:p.Val343=
|
|
ENST00000683557.1:c.715-26G>T
|
ENSP00000508029.1:n.715-26G>T
|
|
ENST00000367282.6:c.1098G>T
MANE Select
|
ENSP00000356251.4:p.Val366=
|
|
ENST00000367282.5:c.1098G>T
|
ENSP00000356251.4:p.Val366=
|
|
NM_004767.3:c.1098G>T
|
NP_004758.3:p.Val366=
|
|
XM_011510158.1:c.537G>T
|
XP_011508460.1:p.Val179=
|
|
NM_004767.4:c.1098G>T
|
NP_004758.3:p.Val366=
|
|
XM_011510158.2:c.537G>T
|
XP_011508460.1:p.Val179=
|
|
NM_004767.5:c.1098G>T
MANE Select
|
NP_004758.3:p.Val366=
|
|