ENST00000216968.5:c.602-6C>T
MANE Select
|
ENSP00000216968.3:n.602-6C>T
|
|
ENST00000216968.4:c.602-6C>T
|
ENSP00000216968.3:n.602-6C>T
|
|
ENST00000634509.1:c.94+246C>T
|
ENSP00000489456.1:n.94+246C>T
|
|
ENST00000635377.1:c.501+246C>T
|
|
|
NM_006404.4:c.602-6C>T
|
NP_006395.2:n.602-6C>T
|
|
XM_011528496.1:c.601+246C>T
|
XP_011526798.1:n.601+246C>T
|
|
NM_001355008.1:c.-101-10821G>A
|
NP_001341937.1:n.-101-10821G>A
|
|
NM_006404.5:c.602-6C>T
MANE Select
|
NP_006395.2:n.602-6C>T
|
|
NM_001355008.2:c.-101-10821G>A
|
NP_001341937.1:n.-101-10821G>A
|
|