NM_016213.5:c.1165C>T
MANE Select
|
NP_057297.2:p.Pro389Ser
|
ENST00000261884.8:c.1165C>T
MANE Select
|
ENSP00000261884.3:p.Pro389Ser
|
NM_001321924.1:c.475C>T
|
NP_001308853.1:p.Pro159Ser
|
NM_001321924.2:c.475C>T
|
NP_001308853.1:p.Pro159Ser
|
NM_016213.4:c.1165C>T
|
NP_057297.2:p.Pro389Ser
|
NR_135855.1:n.1104-4335C>T
|
|
NR_135855.2:n.1072-4335C>T
|
|
ENST00000261884.7:c.1165C>T
|
ENSP00000261884.3:p.Pro389Ser
|
ENST00000560475.1:c.111+4378C>T
|
|
ENST00000560567.5:c.1044-4335C>T
|
ENSP00000453106.1:n.1044-4335C>T
|
XM_005254789.1:c.475C>T
|
XP_005254846.1:p.Pro159Ser
|
XR_243130.1:n.1102-4335C>T
|
|