|
NM_000732.6:c.453C>T
MANE Select
|
NP_000723.1:p.Pro151=
|
|
ENST00000300692.9:c.453C>T
MANE Select
|
ENSP00000300692.4:p.Pro151=
|
|
NM_000732.4:c.453C>T , LRG_37t1:c.453C>T
|
NP_000723.1:p.Pro151=
|
|
NM_001040651.1:c.321C>T
|
NP_001035741.1:p.Pro107=
|
|
NM_001040651.2:c.321C>T
|
NP_001035741.1:p.Pro107=
|
|
ENST00000300692.8:c.453C>T
|
ENSP00000300692.4:p.Pro151=
|
|
ENST00000392884.2:c.321C>T
|
ENSP00000376622.2:p.Pro107=
|
|
ENST00000526561.1:n.126C>T
|
|
|
ENST00000529594.5:c.234C>T
|
ENSP00000437335.1:p.Pro78=
|
|
ENST00000534687.5:c.334C>T
|
|
|
ENST00000695666.1:n.1220C>T
|
|
|
ENST00000695667.1:n.738C>T
|
|