ENST00000318471.5:c.884G>T
MANE Select
|
ENSP00000315680.3:p.Ser295Ile
|
|
ENST00000541292.6:c.*149G>T
|
ENSP00000441004.1:n.*149G>T
|
|
ENST00000678002.1:c.572G>T
|
|
|
ENST00000678557.1:c.770G>T
|
ENSP00000502962.1:p.Ser257Ile
|
|
ENST00000679286.1:c.764G>T
|
ENSP00000503168.1:p.Ser255Ile
|
|
ENST00000318471.4:c.884G>T
|
ENSP00000315680.3:p.Ser295Ile
|
|
NM_000288.3:c.884G>T
|
NP_000279.1:p.Ser295Ile
|
|
XM_005267019.3:c.770G>T
|
XP_005267076.1:p.Ser257Ile
|
|
XM_006715502.1:c.590G>T
|
XP_006715565.1:p.Ser197Ile
|
|
XM_011535900.1:c.*7G>T
|
XP_011534202.1:n.*7G>T
|
|
XM_005267019.4:c.770G>T
|
XP_005267076.1:p.Ser257Ile
|
|
XM_006715502.2:c.590G>T
|
XP_006715565.1:p.Ser197Ile
|
|
XM_017010934.2:c.*7G>T
|
XP_016866423.1:n.*7G>T
|
|
NM_000288.4:c.884G>T
MANE Select
|
NP_000279.1:p.Ser295Ile
|
|