ENST00000493477.2:n.692A=
|
|
|
ENST00000682162.1:c.218A=
|
ENSP00000508203.1:n.218A=
|
|
ENST00000682567.1:n.266A=
|
|
|
ENST00000683521.1:c.189A=
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ENSP00000506864.1:p.Pro63=
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|
ENST00000684483.1:c.189A=
|
ENSP00000507894.1:p.Pro63=
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|
ENST00000366560.4:c.189A=
MANE Select
|
ENSP00000355518.4:p.Pro63=
|
|
ENST00000366560.3:c.189A=
|
ENSP00000355518.3:p.Pro63=
|
|
ENST00000493477.1:n.302A=
|
|
|
NM_000143.3:c.189A= , LRG_504t1:c.189A=
|
NP_000134.2:p.Pro63=
|
|
XM_011544132.1:c.-40A=
|
XP_011542434.1:n.-40A=
|
|
XM_011544132.2:c.-40A=
|
XP_011542434.1:n.-40A=
|
|
NM_000143.4:c.189A=
MANE Select
|
NP_000134.2:p.Pro63=
|
|