ENST00000289473.11:c.*62G>T
MANE Select
|
ENSP00000289473.4:n.*62G>T
|
|
ENST00000289473.10:c.*62G>T
|
ENSP00000289473.4:n.*62G>T
|
|
ENST00000289473.8:c.*62G>T
|
ENSP00000289473.4:n.*62G>T
|
|
ENST00000398421.6:n.2262G>T
|
|
|
ENST00000455062.2:n.1344G>T
|
|
|
NM_000265.5:c.*62G>T
|
NP_000256.4:n.*62G>T
|
|
XM_005250543.3:c.*156G>T
|
XP_005250600.2:n.*156G>T
|
|
XM_011516498.1:c.*109G>T
|
XP_011514800.1:n.*109G>T
|
|
XM_011516501.1:c.*62G>T
|
XP_011514803.1:n.*62G>T
|
|
NM_000265.6:c.*62G>T
|
NP_000256.4:n.*62G>T
|
|
NM_000265.7:c.*62G>T
MANE Select
|
NP_000256.4:n.*62G>T
|
|