ENST00000682565.1:c.7740C>T
|
ENSP00000507671.1:p.Pro2580=
|
|
ENST00000682801.1:c.7740C>T
|
ENSP00000507862.1:p.Pro2580=
|
|
ENST00000682859.1:c.7740C>T
|
ENSP00000508222.1:p.Pro2580=
|
|
ENST00000683791.1:c.1132C>T
|
|
|
ENST00000684460.1:c.5192C>T
|
|
|
ENST00000684548.1:c.7740C>T
|
ENSP00000507421.1:p.Pro2580=
|
|
ENST00000684590.1:c.2187C>T
|
ENSP00000507376.1:p.Pro729=
|
|
ENST00000684656.1:c.5192C>T
|
|
|
ENST00000613296.6:c.8121C>T
MANE Select
|
ENSP00000482968.1:p.Pro2707=
|
|
ENST00000651434.1:c.896-29695C>T
|
|
|
ENST00000423048.5:c.2952C>T
|
ENSP00000399833.1:p.Pro984=
|
|
ENST00000484298.5:c.7995C>T
|
ENSP00000478155.1:p.Pro2665=
|
|
ENST00000613296.4:c.8121C>T
|
ENSP00000482968.1:p.Pro2707=
|
|
ENST00000614410.4:c.8121C>T
|
ENSP00000479094.1:p.Pro2707=
|
|
ENST00000620466.4:n.1924C>T
|
|
|
NM_015120.4:c.8124C>T , LRG_741t1:c.8124C>T
|
NP_055935.4:p.Pro2708=
|
|
NM_001378454.1:c.8121C>T
MANE Select
|
NP_001365383.1:p.Pro2707=
|
|