ENST00000298854.7:c.*145G>C
MANE Select
|
ENSP00000298854.2:n.*145G>C
|
|
ENST00000298854.6:c.*145G>C
|
ENSP00000298854.2:n.*145G>C
|
|
ENST00000352508.7:c.*145G>C
|
ENSP00000298853.3:n.*145G>C
|
|
ENST00000524487.5:c.*145G>C
|
ENSP00000435551.2:n.*145G>C
|
|
ENST00000528356.1:n.339G>C
|
|
|
NM_005055.4:c.*145G>C
|
NP_005046.2:n.*145G>C
|
|
NM_032645.4:c.*145G>C
|
NP_116034.2:n.*145G>C
|
|
XM_011520252.1:c.1469G>C
|
XP_011518554.1:p.Gly490Ala
|
|
NM_005055.5:c.*145G>C
MANE Select
|
NP_005046.2:n.*145G>C
|
|
NM_032645.5:c.*145G>C
|
NP_116034.2:n.*145G>C
|
|