ENST00000267845.8:c.1672C>T
MANE Select
|
ENSP00000267845.3:p.Pro558Ser
|
|
ENST00000267845.7:c.1672C>T
|
ENSP00000267845.3:p.Pro558Ser
|
|
ENST00000543581.5:c.1573C>T
|
ENSP00000440252.1:p.Pro525Ser
|
|
ENST00000559816.1:n.1416C>T
|
|
|
NM_001306146.1:c.1573C>T
|
NP_001293075.1:p.Pro525Ser
|
|
NM_002112.3:c.1672C>T
|
NP_002103.2:p.Pro558Ser
|
|
XM_011521479.1:c.1435C>T
|
XP_011519781.1:p.Pro479Ser
|
|
XM_011521480.1:c.1240C>T
|
XP_011519782.1:p.Pro414Ser
|
|
XM_017022094.1:c.1777C>T
|
XP_016877583.1:p.Pro593Ser
|
|
XM_017022095.1:c.1678C>T
|
XP_016877584.1:p.Pro560Ser
|
|
XM_017022096.1:c.1549C>T
|
XP_016877585.1:p.Pro517Ser
|
|
XM_017022097.1:c.1540C>T
|
XP_016877586.1:p.Pro514Ser
|
|
XM_017022098.1:c.1345C>T
|
XP_016877587.1:p.Pro449Ser
|
|
NM_002112.4:c.1672C>T
MANE Select
|
NP_002103.2:p.Pro558Ser
|
|
NM_001306146.2:c.1573C>T
|
NP_001293075.1:p.Pro525Ser
|
|