ENST00000393943.10:c.-258T=
MANE Select
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ENSP00000377517.4:n.-258T=
|
|
ENST00000635916.2:n.518T=
|
|
|
ENST00000638112.1:c.-247-11T=
|
ENSP00000489839.1:n.-247-11T=
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ENST00000023897.10:c.-247-11T=
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ENSP00000023897.6:n.-247-11T=
|
|
ENST00000393943.9:c.-258T=
|
ENSP00000377517.4:n.-258T=
|
|
ENST00000428797.7:c.-247-11T=
|
ENSP00000393097.2:n.-247-11T=
|
|
ENST00000635096.1:c.-247-11T=
|
ENSP00000489033.1:n.-247-11T=
|
|
NM_000806.5:c.-247-11T=
|
NP_000797.2:n.-247-11T=
|
|
NM_001127643.1:c.-247-11T=
|
NP_001121115.1:n.-247-11T=
|
|
NM_001127644.1:c.-258T=
|
NP_001121116.1:n.-258T=
|
|
XR_941158.3:n.89+2340A=
|
|
|
NM_001127644.2:c.-258T=
MANE Select
|
NP_001121116.1:n.-258T=
|
|
NM_001127643.2:c.-247-11T=
|
NP_001121115.1:n.-247-11T=
|
|