ENST00000682357.1:c.*657G>T
|
ENSP00000507826.1:n.*657G>T
|
|
ENST00000251081.8:c.*865G>T
|
ENSP00000251081.6:n.*865G>T
|
|
ENST00000280904.11:c.*657G>T
MANE Select
|
ENSP00000280904.6:n.*657G>T
|
|
ENST00000648081.1:c.*657G>T
|
ENSP00000497441.1:n.*657G>T
|
|
ENST00000251081.6:c.*865G>T
|
ENSP00000251081.6:n.*865G>T
|
|
ENST00000280904.10:c.*657G>T
|
ENSP00000280904.6:n.*657G>T
|
|
NM_004949.4:c.*865G>T
|
NP_004940.1:n.*865G>T
|
|
NM_024422.4:c.*657G>T
|
NP_077740.1:n.*657G>T
|
|
XM_005258206.3:c.*657G>T
|
XP_005258263.1:n.*657G>T
|
|
XM_005258206.4:c.*657G>T
|
XP_005258263.1:n.*657G>T
|
|
NM_004949.5:c.*865G>T
|
NP_004940.1:n.*865G>T
|
|
NM_024422.6:c.*657G>T
MANE Select
|
NP_077740.1:n.*657G>T
|
|