|
NM_005630.3:c.621C>A
MANE Select
|
NP_005621.2:p.Tyr207Ter
|
|
ENST00000310926.11:c.621C>A
MANE Select
|
ENSP00000311291.4:p.Tyr207Ter
|
|
NM_005630.2:c.621C>A
|
NP_005621.2:p.Tyr207Ter
|
|
ENST00000310926.8:c.621C>A
|
ENSP00000311291.4:p.Tyr207Ter
|
|
ENST00000462770.5:n.521-6270C>A
|
|
|
ENST00000464676.5:n.883C>A
|
|
|
ENST00000481359.3:c.621C>A
|
ENSP00000420028.3:p.Tyr207Ter
|
|
ENST00000493729.5:c.398-1209C>A
|
ENSP00000418893.1:n.398-1209C>A
|
|
XM_011513090.1:c.621C>A
|
XP_011511392.1:p.Tyr207Ter
|
|
XM_017007077.1:c.117C>A
|
XP_016862566.1:p.Tyr39Ter
|
|
XM_024453721.1:c.621C>A
|
XP_024309489.1:p.Tyr207Ter
|