ENST00000682422.1:n.844G>C
|
|
|
ENST00000682545.1:c.*269G>C
|
ENSP00000508402.1:n.*269G>C
|
|
ENST00000682887.1:c.1664G>C
|
ENSP00000506946.1:n.1664G>C
|
|
ENST00000683302.1:c.1194G>C
|
ENSP00000507885.1:p.Arg398Ser
|
|
ENST00000683557.1:c.*95G>C
|
ENSP00000508029.1:n.*95G>C
|
|
ENST00000367282.6:c.1263G>C
MANE Select
|
ENSP00000356251.4:p.Arg421Ser
|
|
ENST00000367282.5:c.1263G>C
|
ENSP00000356251.4:p.Arg421Ser
|
|
NM_004767.3:c.1263G>C
|
NP_004758.3:p.Arg421Ser
|
|
XM_011510158.1:c.702G>C
|
XP_011508460.1:p.Arg234Ser
|
|
NM_004767.4:c.1263G>C
|
NP_004758.3:p.Arg421Ser
|
|
XM_011510158.2:c.702G>C
|
XP_011508460.1:p.Arg234Ser
|
|
NM_004767.5:c.1263G>C
MANE Select
|
NP_004758.3:p.Arg421Ser
|
|