ENST00000480152.3:c.334-413T=
|
ENSP00000483569.2:n.334-413T=
|
|
ENST00000635816.2:c.334-413T=
|
ENSP00000489707.1:n.334-413T=
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|
ENST00000636056.2:c.334-413T=
|
ENSP00000490273.1:n.334-413T=
|
|
ENST00000372037.8:c.334-413T=
MANE Select
|
ENSP00000361107.2:n.334-413T=
|
|
ENST00000635816.1:c.334-413T=
|
ENSP00000489707.1:n.334-413T=
|
|
ENST00000636056.1:c.334-413T=
|
ENSP00000490273.1:n.334-413T=
|
|
ENST00000638429.1:c.334-413T=
|
ENSP00000492290.1:n.334-413T=
|
|
ENST00000372037.7:c.334-413T=
|
ENSP00000361107.1:n.334-413T=
|
|
NM_004329.2:c.334-413T= , LRG_298t1:c.334-413T=
|
NP_004320.2:n.334-413T=
|
|
XM_011540103.1:c.334-413T=
|
XP_011538405.1:n.334-413T=
|
|
XM_011540104.1:c.334-413T=
|
XP_011538406.1:n.334-413T=
|
|
XM_011540103.2:c.334-413T=
|
XP_011538405.1:n.334-413T=
|
|
XM_011540104.2:c.334-413T=
|
XP_011538406.1:n.334-413T=
|
|
NM_004329.3:c.334-413T=
MANE Select
|
NP_004320.2:n.334-413T=
|
|