ENST00000650516.2:c.853+522A=
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ENSP00000498052.2:n.853+522A=
|
|
ENST00000343257.7:c.780A=
MANE Select
|
ENSP00000339867.2:p.Pro260=
|
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ENST00000432192.6:c.604A=
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|
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ENST00000455478.6:c.368A=
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ENSP00000400027.2:n.368A=
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ENST00000650516.1:c.853+522A=
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ENSP00000498052.1:n.853+522A=
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|
ENST00000343257.6:c.780A=
|
ENSP00000339867.2:p.Pro260=
|
|
ENST00000432192.5:c.294A=
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|
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ENST00000455478.5:c.372A=
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|
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ENST00000495612.1:n.154+2571A=
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NM_000083.2:c.780A=
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NP_000074.2:p.Pro260=
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|
NR_046453.1:n.870A=
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|
|
XM_011515781.1:c.853+522A=
|
XP_011514083.1:n.853+522A=
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|
XM_017011739.1:c.403+2571A=
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XP_016867228.1:n.403+2571A=
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|
XM_017011740.1:c.403+2571A=
|
XP_016867229.1:n.403+2571A=
|
|
NM_000083.3:c.780A=
MANE Select
|
NP_000074.3:p.Pro260=
|
|
NR_046453.2:n.885A=
|
|
|