ENST00000324727.9:c.529C>A
MANE Select
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ENSP00000322460.4:p.Leu177Ile
|
|
ENST00000324727.8:c.529C>A
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ENSP00000322460.4:p.Leu177Ile
|
|
ENST00000415030.6:n.672C>A
|
|
|
ENST00000423160.2:n.163C>A
|
|
|
ENST00000529878.1:c.127C>A
|
ENSP00000436343.1:p.Leu43Ile
|
|
ENST00000531550.1:n.594C>A
|
|
|
ENST00000532138.1:n.785C>A
|
|
|
NM_001142348.1:c.127C>A
|
NP_001135820.1:p.Leu43Ile
|
|
NM_001142349.1:c.199C>A
|
NP_001135821.1:p.Leu67Ile
|
|
NM_174934.3:c.529C>A , LRG_330t1:c.529C>A
|
NP_777594.1:p.Leu177Ile
|
|
NR_024527.1:n.554C>A
|
|
|
NM_001142348.2:c.127C>A
|
NP_001135820.1:p.Leu43Ile
|
|
NM_001142349.2:c.199C>A
|
NP_001135821.1:p.Leu67Ile
|
|
NR_024527.2:n.518C>A
|
|
|
NM_174934.4:c.529C>A
MANE Select
|
NP_777594.1:p.Leu177Ile
|
|